← Back to catalogue

Inhance

FDA UDI

Class II (US FDA UDI)

by Depuy (ireland)

Identity

Trade Name
INHANCE FDA UDI
Generic Name
Total reverse shoulder prosthesis FDA UDI
Device Name
INHANCE SHOULDER SYSTEM REVERSE LINER RETENTIVE X-LINKED VITAMIN E PE Ø40+4mm FDA UDI
Model / Reference
5500-40-104 FDA UDI
Description
INHANCE SHOULDER SYSTEM REVERSE LINER RETENTIVE X-LINKED VITAMIN E PE Ø40+4mm FDA UDI

Identifiers

Catalog Number
550040104 FDA UDI
Primary DI / UDI-DI
10603295546498 FDA UDI
510(k) Number
K212737 FDA UDI
FDA Product Code
KWS FDA UDI
HSD FDA UDI
MBF FDA UDI
PHX FDA UDI
KWT FDA UDI
PAO FDA UDI
GMDN Term
Total reverse shoulder prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3660 FDA UDI
888.3690 FDA UDI
888.3670 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: Total reverse shoulder prosthesis

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

Similar devices

Also classified as Total reverse shoulder prosthesis.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Depuy (ireland)

Sources (1)

  • FDA UDI 2c5c6b53-4e14-448f-8076-a2bef83d8130 36 fields · synced May 30, 2026