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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 body FDA UDI
Device Name
INHANCE SHOULDER SYSTEM REVERSE HUMERAL SHELL X-SMALL Ø28+0mm FDA UDI
Model / Reference
5500-00-280 FDA UDI
Description
INHANCE SHOULDER SYSTEM REVERSE HUMERAL SHELL X-SMALL Ø28+0mm FDA UDI

Identifiers

Catalog Number
550000280 FDA UDI
Primary DI / UDI-DI
10603295547037 FDA UDI
510(k) Number
K212737 FDA UDI
FDA Product Code
MBF FDA UDI
KWS FDA UDI
HSD FDA UDI
PAO FDA UDI
KWT FDA UDI
PHX FDA UDI
GMDN Term
Reverse shoulder prosthesis body FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3670 FDA UDI
888.3660 FDA UDI
888.3690 FDA UDI
888.3650 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 body

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

Similar devices

Also classified as Reverse shoulder prosthesis body.

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 22f7c3da-4bba-43b2-a0f4-321c417efe06 36 fields · synced May 30, 2026