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Inhance

FDA UDI

Class II (US FDA UDI)

by Depuy (ireland)

Identity

Trade Name
INHANCE FDA UDI
Generic Name
Humeral metaphyseal anchor FDA UDI
Device Name
INHANCE SHOULDER SYSTEM STEMLESS X-SMALL DIAMETER 28mm CEMENTLESS FDA UDI
Model / Reference
5200-00-028 FDA UDI
Description
INHANCE SHOULDER SYSTEM STEMLESS X-SMALL DIAMETER 28mm CEMENTLESS FDA UDI

Identifiers

Catalog Number
520000028 FDA UDI
Primary DI / UDI-DI
10603295538271 FDA UDI
FDA Product Code
PKC FDA UDI
PAO FDA UDI
GMDN Term
Humeral metaphyseal anchor FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3660 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
MRI Safety
MR Conditional FDA UDI

Category: Humeral metaphyseal anchor

Inhance by Depuy (ireland) — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Humeral metaphyseal anchor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Depuy (ireland)

Sources (1)

  • FDA UDI 4742ecd0-93bc-42b5-9462-b6d8ab2cdeaf 35 fields · synced Jun 6, 2026