Device manufacturer, as written on reports

Depuy-Raynham A Div Of Depuy Orthopaedics: medical device reports filed with FDA

1,261 reports name it as the manufacturer of the device involved, 2000–2014.

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.

1,261
reports naming it as manufacturer: 0% of all MAUDE reports; 0
reports, 12 months to August 2026: 0 in the 12 months before; 7.1%
classified as malfunction: 62.3% across all reports; 0%
classified as death, as reported: 0.9% across all reports

1,261 medical device reports received by FDA give Depuy-Raynham A Div Of Depuy Orthopaedics as the manufacturer of the device involved, 0% of the MAUDE database, from February 2000 to April 2014. 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 (92.7%) and malfunction (7.1%). 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
Lcs Comp Rp Insert Std+ 10mm	Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing	26	3	0%
Lcs Comp Rp Insert Lg 10mm	Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing	23	1	0%
Pinn Can Bone Screw 6 5mmx25mm	Prosthesis, hip, semi-constrained, metal/polymer, porous uncemented	20	32	0%
Pinn Can Bone Screw 6 5mmx20mm	Prosthesis, hip, semi-constrained, metal/polymer, porous uncemented	13	19	0.3%
Lcs Comp Rp Insert Std 10mm	Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing	12	7	0%
Pfc Keel Tib Tray Cem Sz3	Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer/metal/polymer	11	0	0%
Pinn Can Bone Screw 6 5mmx30mm	Prosthesis, hip, semi-constrained, metal/polymer, porous uncemented	11	22	0.3%
Pinn Can Bone Screw 6 5mmx35mm	Prosthesis, hip, semi-constrained, metal/polymer, porous uncemented	11	21	0%
Pinn Can Bone Screw 6 5mmx15mm	Prosthesis, hip, semi-constrained, metal/polymer, porous uncemented	6	16	0.6%
Sig Mod Tib Tray Cem Cocr 2 5	Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer/metal/polymer	6	2	0.2%
Pfc Sigma Mod Tib Tray Cem Sz4	Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer/metal/polymer	5	0	0%
Pfc Sigma Tib Tray Cem Sz3	Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer/metal/polymer	5	0	0%
Pfc Sigma/Ov/Dome Pat 3peg 38	Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer/metal/polymer	5	3	0.4%
Pfc Sigma/Ov/Dome Pat 3peg 41	Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer/metal/polymer	4	4	0%
Hp Mbt Cem Keel Punch Sz 4-7	Orthopedic manual surgical instrument	3	0	0%
Universal Stem 75x16mm Fluted	Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer/metal/polymer	3	3	0%
Pfc Sigmarp Stb Tb In 4 10 0	Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing	2	5	0%
Pinn Can Bone Screw 6 5mmx40mm	Prosthesis, hip, semi-constrained, metal/polymer, porous uncemented	2	3	0%
Glenosphere Orientation Guide	Orthopedic manual surgical instrument	1	13	0%
Mbt Cem Keel Tib Tray Sz3	Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing	1	9	0%
Sigma Hp Fem Notch Impactor	Impactor	1	8	0%
Sp 2 Femoral Impactor	Impactor	1	2	0%
Sp2 Tibial Radel Impactor	Impactor	1	2	0%

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
JWH	Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer/metal/polymer	647	51.3%
NJL	Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing	185	14.7%
LXH	Orthopedic manual surgical instrument	90	7.1%
NDJ	Screw, fixation, bone, non-spinal, metallic	79	6.3%
JDI	Prosthesis, hip, semi-constrained, metal/polymer, cemented	39	3.1%
HRY	Prosthesis, knee, femorotibial, semi-constrained, cemented, metal/polymer	36	2.9%
HSH	Prosthesis, knee, hemi-, tibial, resurfacing (uncemented)	36	2.9%
KRO	Prosthesis, knee, femorotibial, constrained, cemented, metal/polymer	21	1.7%
HSA	Prosthesis, knee, hemi-, femoral	17	1.3%
KWA	Prosthesis, hip, semi-constrained (metal uncemented acetabular component)	16	1.3%

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%0

Injury92.7%1,169

Malfunction7.1%89

Other0%0

Not given0.2%3

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

Questions about Depuy-Raynham A Div Of Depuy Orthopaedics reports

How many FDA device reports name Depuy-Raynham A Div Of Depuy Orthopaedics as manufacturer?

1,261 reports through August 2026, 0 of them in the latest 12 months.

Which of its brands appear most often?

Lcs Comp Rp Insert Std+ 10mm (26), Lcs Comp Rp Insert Lg 10mm (23), Pinn Can Bone Screw 6 5mmx25mm (20), Pinn Can Bone Screw 6 5mmx20mm (13) and Lcs Comp Rp Insert Std 10mm (12).

Which device types does it report on?

prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer/metal/polymer (51.3%), prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing (14.7%), orthopedic manual surgical instrument (7.1%) and screw, fixation, bone, non-spinal, metallic (6.3%).

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.