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Humeris Shoulder

FDA UDI

Class II (US FDA UDI)

by Fx Solutions

Identity

Trade Name
Humeris Shoulder FDA UDI
Generic Name
Shoulder humeral body prosthesis FDA UDI
Device Name
CENTERED SPACER TA6V Ø39 +5 mm 0° FDA UDI
Model / Reference
106-3905 FDA UDI
Description
CENTERED SPACER TA6V Ø39 +5 mm 0° FDA UDI

Identifiers

Catalog Number
106-3905 FDA UDI
Primary DI / UDI-DI
03701037300565 FDA UDI
510(k) Number
K163669 FDA UDI
FDA Product Code
HSD FDA UDI
GMDN Term
Shoulder humeral body prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 39 Millimeter FDA UDI

Category: Shoulder humeral body prosthesis

Humeris Shoulder by Fx Solutions — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Shoulder humeral body prosthesis.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Fx Solutions

Sources (1)

  • FDA UDI 8a98eb83-40bb-48f7-8118-4ccc976855cf 37 fields · synced May 30, 2026