Device manufacturer, as written on reports

8010379 Depuy Intl: medical device reports filed with FDA

1,527 reports name it as the manufacturer of the device involved, 2011–2017.

Read first · FDA's statement on these data

Adverse event reports submitted to FDA do not undergo extensive validation or verification. Therefore, a causal relationship cannot be established between product and reactions listed in a report. While a suspected relationship may exist, it is not medically validated and should not be the sole source of information for clinical decision making or other assumptions about the safety or efficacy of a product. Additionally, it is important to remember that adverse event reports represent a small percentage of total usage numbers of a product. Common products may have a higher number of adverse events due to the higher total number of people using the product. openFDA, FDA

FDA adds: "Although MDRs are a valuable source of information, this passive surveillance system has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data. In addition, the incidence or prevalence of an event cannot be determined from this reporting system alone due to potential under-reporting of events and lack of information about frequency of device use." And: "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices."

Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated.

Not medical advice. This site counts what was reported to FDA. Questions about a medicine or device belong with a pharmacist or clinician.

1,527
reports naming it as manufacturer: 0% of all MAUDE reports; 0
reports, 12 months to August 2026: 0 in the 12 months before; 0.1%
classified as malfunction: 62.3% across all reports; 0.1%
classified as death, as reported: 0.9% across all reports

1,527 medical device reports received by FDA give 8010379 Depuy Intl as the manufacturer of the device involved, 0% of the MAUDE database, from March 2011 to January 2017. Manufacturer names are as written on the report; subsidiaries and spelling variants may appear as separate names.

0 reports arrived in the 12 months to August 2026, and none in the 12 months before. FDA releases MAUDE data monthly; reports can arrive months after an event, so the newest months grow in later releases. The event types recorded are injury (99.8%), death (0.1%) and malfunction (0.1%). Manufacturers are required to report events they learn of, so a large manufacturer with many products in use files many reports. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data."

Brands named most often

Brand	Device type	Reports	Latest 12 months	Classified as death
Pinnacle Mtl Ins Neut36idx52od	Prosthesis, hip, semi-constrained (metal uncemented acetabular component)	112	13	0.1%
Articuleze M Head 36mm +1 5	Prosthesis, hip, semi-constrained, metal/polymer, cemented	104	24	0.1%
Articuleze M Head 36mm +5	Prosthesis, hip, semi-constrained, metal/polymer, cemented	104	24	0.1%
Pinnacle Mtl Ins Neut36idx54od	Prosthesis, hip, semi-constrained (metal uncemented acetabular component)	93	11	0.1%
Articuleze M Head 36mm +8 5	Prosthesis, hip, semi-constrained, metal/polymer, cemented	64	11	0.1%
Pinnacle Mtl Ins Neut36idx50od	Prosthesis, hip, semi-constrained (metal uncemented acetabular component)	63	9	0%
Articuleze M Head 36mm -2	Prosthesis, hip, semi-constrained, metal/polymer, cemented	43	10	0.2%
Pinnacle Mtl Ins Neut36idx56od	Prosthesis, hip, semi-constrained (metal uncemented acetabular component)	35	5	0.2%
Pinnacle Mtl Ins Neut40idx56od	Prosthesis, hip, semi-constrained (metal uncemented acetabular component)	31	6	0.1%
Unknown Depuy Femoral Head	Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented	26	0	0.1%
Articuleze M Head 36mm +12	Prosthesis, hip, semi-constrained, metal/polymer, cemented	23	2	0%
Pinnacle Mtl Ins Neut36idx58od	Prosthesis, hip, semi-constrained (metal uncemented acetabular component)	23	1	0.2%
12/14 Articul 40mm M Spec+1 5	Prosthesis, hip, semi-constrained, metal/polymer, cemented	21	9	0.2%
Adapter Sleeves 12/14 +2	Prosthesis, hip, semi-constrained (metal uncemented acetabular component)	19	5	0.4%
S-Rom M Head 36mm +0	Prosthesis, hip, semi-constrained, metal/polymer, cemented	16	0	0%
12/14 Articul 40mm M Spec+5	Prosthesis, hip, semi-constrained, metal/polymer, cemented	14	0	0%
S-Rom M Head 36mm +3	Prosthesis, hip, semi-constrained, metal/polymer, cemented	14	0	0%
Pinnacle Mtl Ins Neut40idx58od	Prosthesis, hip, semi-constrained (metal uncemented acetabular component)	13	0	0.3%
Pinnacle Mtl Ins Neut40idx60od	Prosthesis, hip, semi-constrained (metal uncemented acetabular component)	13	0	0%
Articuleze M Head 36mm +15 5	Prosthesis, hip, semi-constrained, metal/polymer, cemented	12	0	0%
12/14 Articul 40mm M Spec+8 5	Prosthesis, hip, semi-constrained, metal/polymer, cemented	11	4	0.2%
Pinnacle Mtl Ins Neut36idx60od	Prosthesis, hip, semi-constrained (metal uncemented acetabular component)	10	0	0.4%
Asr Acetabular Cups 58	Prosthesis, hip, semi-constrained (metal uncemented acetabular component)	9	1	0.5%
S-Rom M Head 36mm +6	Prosthesis, hip, semi-constrained, metal/polymer, cemented	9	0	0%
Unknown Depuy Pinnacle Metal Liner	Prosthesis, hip, semi-constrained (metal uncemented acetabular component)	9	0	0.3%
12/14 Articul 40mm M Spec-2	Prosthesis, hip, semi-constrained, metal/polymer, cemented	8	1	0%
Articul/Eze Ball 28 +1 5 Gr	Prosthesis, hip, semi-constrained, metal/polymer, cemented	8	20	0.3%
Asr Uni Femoral Impl Size 49	Prosthesis, hip, semi-constrained (metal uncemented acetabular component)	8	0	0.4%
Adapter Sleeves 12/14 +5	Prosthesis, hip, semi-constrained (metal uncemented acetabular component)	7	0	0.5%
Articul/Eze Ball 28 +5 Br	Prosthesis, hip, semi-constrained, metal/polymer, cemented	7	14	0.2%

Brands with a page on this site, ordered by report count for navigation only. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data."

Device types

Product code	Device type	Reports	Share
KWA	Prosthesis, hip, semi-constrained (metal uncemented acetabular component)	748	49%
JDI	Prosthesis, hip, semi-constrained, metal/polymer, cemented	543	35.6%
LPH	Prosthesis, hip, semi-constrained, metal/polymer, porous uncemented	134	8.8%
KWY	Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented	29	1.9%
LZO	Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented	29	1.9%
KXA	Prosthesis, hip, femoral, resurfacing	8	0.5%
JDG	Prosthesis, hip, femoral component, cemented, metal	7	0.5%
JWH	Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer/metal/polymer	6	0.4%
NJL	Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing	5	0.3%
HRY	Prosthesis, knee, femorotibial, semi-constrained, cemented, metal/polymer	3	0.2%

Reports by month, five years

FDA releases MAUDE data monthly; reports can arrive months after an event, so the newest months grow in later releases.

Event type

Death0.1%2

Injury99.8%1,524

Malfunction0.1%1

Other0%0

Not given0%0

Grey bar: all 26,136,888 MAUDE reports. Event type is the filer's classification and is not verified by FDA.

Questions about 8010379 Depuy Intl reports

How many FDA device reports name 8010379 Depuy Intl as manufacturer?

1,527 reports through August 2026, 0 of them in the latest 12 months.

Which of its brands appear most often?

Pinnacle Mtl Ins Neut36idx52od (112), Articuleze M Head 36mm +1 5 (104), Articuleze M Head 36mm +5 (104), Pinnacle Mtl Ins Neut36idx54od (93) and Articuleze M Head 36mm +8 5 (64).

Which device types does it report on?

prosthesis, hip, semi-constrained (metal uncemented acetabular component) (49%), prosthesis, hip, semi-constrained, metal/polymer, cemented (35.6%), prosthesis, hip, semi-constrained, metal/polymer, porous uncemented (8.8%) and prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented (1.9%).

Does a high count say something about the manufacturer?

Not by itself. Manufacturers must file a report for every event they become aware of, so report volume follows the number of devices in use. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data."

Where this comes from. Counts are built from the openFDA Device Adverse Event (MAUDE) bulk export released 28 Sep 2026, which holds reports FDA received through 31 Aug 2026. Brand, generic and manufacturer names are as written on the reports; product code names come from FDA's device classification. Manufacturer names are pooled after company suffixes (Inc., LLC, GmbH and similar) are dropped; names that read as a person rather than an organisation are never published. No report narrative, lot number, patient detail or reporter identity is published. See the methodology and sources; FDA's record is authoritative, and corrections are handled within five working days.

Drug data (FAERS) through 30 Jun 2026; device data (MAUDE) through 31 Aug 2026. Not medical advice.