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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 shell FDA UDI
Device Name
Trinity™ PLUS Ø68 mm Taper Size 5 Shell FDA UDI
Model / Reference
324.05.768 FDA UDI
Description
Trinity™ PLUS Ø68 mm Taper Size 5 Shell FDA UDI

Identifiers

Catalog Number
324.05.768 FDA UDI
Primary DI / UDI-DI
05055343898208 FDA UDI
510(k) Number
K172551 FDA UDI
FDA Product Code
OQG FDA UDI
LZO FDA UDI
OQI FDA UDI
LPH FDA UDI
MBL FDA UDI
GMDN Term
Acetabular shell FDA UDI

Classification

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

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Radiation Sterilization FDA UDI

Category: Acetabular shell

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 shell.

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 70626ab0-5294-488a-921d-2a2bf2e9f1e0 36 fields · synced Jun 1, 2026