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APEX PS Knee

FDA UDI

Class II (US FDA UDI)

by OMNIlife science, Inc.

Identity

Trade Name
APEX PS Knee FDA UDI
Generic Name
Tibial insert FDA UDI
Device Name
PS-C Insert, Size 2 x 11mm FDA UDI
Model / Reference
KP-22211 FDA UDI
Description
PS-C Insert, Size 2 x 11mm FDA UDI

Identifiers

Catalog Number
KP-22211 FDA UDI
Primary DI / UDI-DI
00841690113508 FDA UDI
FDA Product Code
JWH FDA UDI
MBH FDA UDI
GMDN Term
Tibial insert FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3560 FDA UDI
888.3565 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
Ethylene Oxide FDA UDI

Category: Tibial insert

APEX PS Knee by OMNIlife science, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tibial insert.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7553d6a8-4875-42c4-a2d4-c87ded75b3e8 35 fields · synced Jun 9, 2026