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Toe Joint Cobalt Chrome Npc Lg 23mm

FDA UDI

Class II (US FDA UDI)

by Biopro, Inc.

Identity

Trade Name
TOE JOINT COBALT CHROME NPC LG 23MM FDA UDI
Generic Name
Partial metatarsophalangeal joint prosthesis FDA UDI
Model / Reference
10062 FDA UDI

Identifiers

Primary DI / UDI-DI
00810012480024 FDA UDI
510(k) Number
K041595 FDA UDI
FDA Product Code
KWD FDA UDI
GMDN Term
Partial metatarsophalangeal joint prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3730 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

Yes

FDA UDI

Category: Partial metatarsophalangeal joint prosthesis

Toe Joint Cobalt Chrome Npc Lg 23mm by Biopro, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Partial metatarsophalangeal joint prosthesis.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Biopro, Inc.

Sources (1)

  • FDA UDI 307b73a7-ab0d-4876-b99b-78b7cc885a05 33 fields · synced Jun 1, 2026