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Engage Partial Knee System

FDA UDI

Class II (US FDA UDI)

by Engage Uni, LLC

Identity

Trade Name
Engage Partial Knee System FDA UDI
Generic Name
Unicondylar knee prosthesis FDA UDI
Device Name
Femoral Component, Size 5 - Right Medial FDA UDI
Model / Reference
1-10003-500 FDA UDI
Description
Femoral Component, Size 5 - Right Medial FDA UDI

Identifiers

Primary DI / UDI-DI
B6951100035000 FDA UDI
510(k) Number
K190439 FDA UDI
FDA Product Code
NJD FDA UDI
HSX FDA UDI
GMDN Term
Unicondylar knee prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3535 FDA UDI
888.3520 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

Category: Unicondylar knee prosthesis

Engage Partial Knee System by Engage Uni, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Unicondylar knee prosthesis.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Engage Uni, LLC

Sources (1)

  • FDA UDI 4c7f2a4c-3332-4a28-b42f-6056dd13ac62 35 fields · synced May 31, 2026