Device manufacturer, as written on reports

Stryker Orthopaedics Cork: medical device reports filed with FDA

5,049 reports name it as the manufacturer of the device involved, 2004–2015.

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.

5,049
reports naming it as manufacturer: 0% of all MAUDE reports; 0
reports, 12 months to August 2026: 0 in the 12 months before; 20.3%
classified as malfunction: 62.3% across all reports; 0.1%
classified as death, as reported: 0.9% across all reports

5,049 medical device reports received by FDA give Stryker Orthopaedics Cork as the manufacturer of the device involved, 0% of the MAUDE database, from April 2004 to July 2015. 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 (78.8%), malfunction (20.3%) and other (0.9%). 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
Trident Alumina Insert	Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented	211	0	0%
Abgii Modular Stem	Prosthesis, hip, semi-constrained, uncemented, metal / polymer, non-porous, calcium phosphate	97	1	0.5%
Trident Hemispherical Cluster Hole Shell	Prosthesis, hip, semi-constrained, uncemented, metal / polymer, non-porous, calcium phosphate	64	0	0%
Accolade Plus Tmzf Hip Stem 3	Prosthesis, hip, semi-constrained, metal/polymer, porous uncemented	30	5	0%
Unknown Product	Stretcher, wheeled	23	0	2.7%
Exeter V40 Stem 44mm No 0	Prosthesis, hip, semi-constrained, metal/polymer, cemented	19	8	0%
Accolade Plus Tmzf Hip Stem 4	Prosthesis, hip, semi-constrained, metal/polymer, porous uncemented	18	6	0%
Restoration Adm X3 Ins 28/52	Prosthesis, hip, semi-constrained, uncemented, metal / polymer, non-porous, calcium phosphate	15	5	0%
Accolade	Implantable pulse generator, pacemaker (non-crt)	9	4	1.5%
Restoration Adm X3 Ins 28/48	Prosthesis, hip, semi-constrained, uncemented, metal / polymer, non-porous, calcium phosphate	9	6	0%
Modular Dual Mobility Insert	Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented	7	6	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
MEH	Prosthesis, hip, semi-constrained, uncemented, metal / polymer, non-porous, calcium phosphate	2,278	45.1%
JDI	Prosthesis, hip, semi-constrained, metal/polymer, cemented	607	12%
LZO	Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented	581	11.5%
MRA	Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented	374	7.4%
KWY	Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented	248	4.9%
JWH	Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer/metal/polymer	211	4.2%
LPH	Prosthesis, hip, semi-constrained, metal/polymer, porous uncemented	206	4.1%
HSH	Prosthesis, knee, hemi-, tibial, resurfacing (uncemented)	145	2.9%
LXH	Orthopedic manual surgical instrument	97	1.9%
KWB	Prosthesis, hip, hemi-, acetabular, cemented, metal	56	1.1%

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%3

Injury78.8%3,978

Malfunction20.3%1,024

Other0.9%43

Not given0%1

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

Questions about Stryker Orthopaedics Cork reports

How many FDA device reports name Stryker Orthopaedics Cork as manufacturer?

5,049 reports through August 2026, 0 of them in the latest 12 months.

Which of its brands appear most often?

Trident Alumina Insert (211), Abgii Modular Stem (97), Trident Hemispherical Cluster Hole Shell (64), Accolade Plus Tmzf Hip Stem 3 (30) and Unknown Product (23).

Which device types does it report on?

prosthesis, hip, semi-constrained, uncemented, metal / polymer, non-porous, calcium phosphate (45.1%), prosthesis, hip, semi-constrained, metal/polymer, cemented (12%), prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented (11.5%) and prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented (7.4%).

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.