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Corin Medical

Country not established

Devices
1
FDA recalls
11 ongoing

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA recalls

What Corin Medical makes

Corin Medical manufactures the Trinity Acetabular System, a medical device used in hip replacement surgeries to provide a stable acetabular component for total hip arthroplasty.

The Trinity Acetabular System is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.

AI-generated from registry data, 26 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Trinity Acetabular System Ref K130128

    Active Regimes: 510(k) Registry: 510(k) Class:II

FDA recalls1

Recalls are matched to the firm by name. FDA recall data as of 22 Oct 2026.

FDA recall records list 1 recall initiated by Corin Medical, initiated on 2025-05-23. By recorded status: 1 ongoing. The reasons filed fall into these groups: packaging. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.

Generated automatically from FDA recall records, as a summary of the records listed below. It describes what the records state and is not an assessment of this manufacturer.

Recalls initiated per year

  • 2017 0
  • 2018 0
  • 2019 0
  • 2020 0
  • 2021 0
  • 2022 0
  • 2023 0
  • 2024 0
  • 2025 1
  • 2026 0
  • 2025

    • 23 May 2025 Z-2069-2025 Class II Ongoing Investigation has identified that the age of the nylon packaging material has caused a loss of integrity of some pouches. Distribution: US Nationwide distribution in the states of CA, CO, FL, IL, OK, TX, UT. Submission numbers: K101994, K153437, K112891

Frequently asked questions

How many devices does Corin Medical have in the registry?

The registry currently lists 1 device for Corin Medical. Devices recorded under merged duplicate company entries are counted once.

Which registries list Corin Medical's devices?

Among its 1 most recently registered device, Corin Medical has devices listed in FDA 510(k) (1 device).

What risk classes do Corin Medical's devices fall under?

Among its 1 most recently registered device, the classes recorded for Corin Medical's devices are Class II. Each device page shows its own class and authorisation.

Are there FDA recall records for Corin Medical?

FDA recall records list 1 recall initiated by Corin Medical, the most recent initiated on 23 May 2025. 1 of them is recorded as ongoing. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.

What are the newest devices from Corin Medical in the registry?

The most recently registered devices listed for Corin Medical include TRINITY ACETABULAR SYSTEM.

Generated automatically from registry data and not verified by a human reviewer.