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Silicone MCP

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
Silicone MCP FDA UDI
Generic Name
Metacarpophalangeal joint prosthesis, one-piece FDA UDI
Device Name
SILICONE MCP SZ 05 FDA UDI
Model / Reference
SMCP-500-05-WW FDA UDI
Description
SILICONE MCP SZ 05 FDA UDI

Identifiers

Catalog Number
SMCP-500-05-WW FDA UDI
Primary DI / UDI-DI
00885556856871 FDA UDI
510(k) Number
K022892 FDA UDI
K233670 FDA UDI
FDA Product Code
KYJ FDA UDI
GMDN Term
Metacarpophalangeal joint prosthesis, one-piece FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3230 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: Metacarpophalangeal joint prosthesis, one-piece

Silicone MCP by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Metacarpophalangeal joint prosthesis, one-piece.

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 6483bfbe-6807-4ad7-ab45-53c18100ccca 36 fields · synced Jun 8, 2026