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Inhance

FDA UDI

Class II (US FDA UDI)

by Depuy (ireland)

Identity

Trade Name
INHANCE FDA UDI
Generic Name
Reverse shoulder prosthesis head FDA UDI
Device Name
INHANCE SHOULDER SYSTEM GLENOSPHERE Ø32+4mm FDA UDI
Model / Reference
5505-32-004 FDA UDI
Description
INHANCE SHOULDER SYSTEM GLENOSPHERE Ø32+4mm FDA UDI

Identifiers

Catalog Number
550532004 FDA UDI
Primary DI / UDI-DI
10603295546665 FDA UDI
510(k) Number
K212737 FDA UDI
FDA Product Code
HSD FDA UDI
PHX FDA UDI
KWT FDA UDI
MBF FDA UDI
PAO FDA UDI
KWS FDA UDI
GMDN Term
Reverse shoulder prosthesis head FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3690 FDA UDI
888.3660 FDA UDI
888.3650 FDA UDI
888.3670 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: Reverse shoulder prosthesis head

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

Similar devices

Also classified as Reverse shoulder prosthesis head.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Depuy (ireland)

Sources (1)

  • FDA UDI e2762313-3441-4cb0-9575-4766ba7ea710 36 fields · synced May 30, 2026