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Shoulder Innovations TSA

FDA UDI

Class II (US FDA UDI)

by SHOULDER INNOVATIONS, Inc

Identity

Trade Name
Shoulder Innovations TSA FDA UDI
Generic Name
Shoulder glenoid fossa prosthesis, prefabricated FDA UDI
Device Name
Shoulder Innovations InSet Plus Glenoid Trial, Circular Center Peg, 24mm x 5°, Stainless Steel FDA UDI
Model / Reference
24 mm x 5° FDA UDI
Description
Shoulder Innovations InSet Plus Glenoid Trial, Circular Center Peg, 24mm x 5°, Stainless Steel FDA UDI

Identifiers

Catalog Number
2N1AC24005 FDA UDI
Primary DI / UDI-DI
B1132N1AC24005 FDA UDI
510(k) Number
K102670 FDA UDI
K110905 FDA UDI
K111596 FDA UDI
FDA Product Code
KWT FDA UDI
KWS FDA UDI
HSD FDA UDI
GMDN Term
Shoulder glenoid fossa prosthesis, prefabricated FDA UDI

Classification

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

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Total shoulder prosthesisShoulder glenoid fossa prosthesis, prefabricated

Shoulder Innovations TSA by SHOULDER INNOVATIONS, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Shoulder glenoid fossa prosthesis, prefabricated.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1ac07ce7-771d-445c-9199-a6e98dd00cc8 36 fields · synced May 30, 2026