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HemiCAPOVO®

FDA UDI

Class II (US FDA UDI)

by Arthrosurface Incorporated

Identity

Trade Name
HemiCAPOVO® FDA UDI
Generic Name
Shoulder prosthesis screw FDA UDI
Device Name
Taper Post, 12.0mm x 32mm, OVO FDA UDI
Model / Reference
8156-0032-W FDA UDI
Description
Taper Post, 12.0mm x 32mm, OVO FDA UDI

Identifiers

Catalog Number
8156-0032-W FDA UDI
Primary DI / UDI-DI
M52881560032W0 FDA UDI
510(k) Number
K142942 FDA UDI
FDA Product Code
HSD FDA UDI
GMDN Term
Shoulder prosthesis screw 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

No

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

Dimensions & Sizes

Size
Outer Diameter — 12 Millimeter FDA UDI

Category: Shoulder prosthesis screw

HemiCAPOVO® by Arthrosurface Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Shoulder prosthesis screw.

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 11918cfc-f284-4f44-9bf2-49654862c1a8 37 fields · synced May 30, 2026