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Veritas rTSA

FDA UDI

Class II (US FDA UDI)

by Restor3D

Identity

Trade Name
Veritas rTSA FDA UDI
Generic Name
Reverse shoulder prosthesis head FDA UDI
Device Name
CoCr Glenosphere w/ Ti Security Screw, 32mm, +2mm FDA UDI
Model / Reference
1501-3202 FDA UDI
Description
CoCr Glenosphere w/ Ti Security Screw, 32mm, +2mm FDA UDI

Identifiers

Primary DI / UDI-DI
00840097515564 FDA UDI
510(k) Number
K243643 FDA UDI
FDA Product Code
PHX FDA UDI
GMDN Term
Reverse shoulder prosthesis head 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

Category: Reverse shoulder prosthesis head

Veritas rTSA by Restor3D — 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
Restor3D

Sources (1)

  • FDA UDI 78ca0cde-7201-479e-9974-69a30f9a5ac9 34 fields · synced Jun 8, 2026