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Corin Trinity™ PLUS Acetabular Shell

FDA UDI

Class II (US FDA UDI)

by Corin Ltd

Identity

Trade Name
Corin Trinity™ PLUS Acetabular Shell FDA UDI
Generic Name
Acetabular orthopaedic reamer FDA UDI
Device Name
Acetabular Reamer - Ø69mm FDA UDI
Model / Reference
299.769 FDA UDI
Description
Acetabular Reamer - Ø69mm FDA UDI

Identifiers

Catalog Number
299.769 FDA UDI
Primary DI / UDI-DI
05055343827987 FDA UDI
510(k) Number
K172551 FDA UDI
FDA Product Code
OQI FDA UDI
LPH FDA UDI
OQG FDA UDI
MBL FDA UDI
LZO FDA UDI
GMDN Term
Acetabular orthopaedic reamer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3353 FDA UDI
888.3358 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Acetabular orthopaedic reamer

Corin Trinity™ PLUS Acetabular Shell by Corin Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Acetabular orthopaedic reamer.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Corin Ltd

Sources (1)

  • FDA UDI 5f6c26e1-9fe3-4f81-91eb-fcdc210fada4 36 fields · synced May 30, 2026