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WishFIX

FDA UDI

Class I (US FDA UDI)

by Wishbone Medical Inc.

Identity

Trade Name
WishFIX FDA UDI
Generic Name
Orthopaedic prosthesis implantation positioning instrument, single-use FDA UDI
Device Name
WishFIX Direct Measurement Device FDA UDI
Model / Reference
51-202-DMD000G-1 FDA UDI
Description
WishFIX Direct Measurement Device FDA UDI

Identifiers

Catalog Number
51-202-DMD000G-1 FDA UDI
Primary DI / UDI-DI
B56251202DMD000G10 FDA UDI
FDA Product Code
FTY FDA UDI
GMDN Term
Orthopaedic prosthesis implantation positioning instrument, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Orthopaedic prosthesis implantation positioning instrument, single-use

WishFIX by Wishbone Medical Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic prosthesis implantation positioning instrument, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Wishbone Medical Inc.

Sources (1)

  • FDA UDI 20085cc2-dd6f-4a6c-8975-94b01c05b0c5 34 fields · synced Jun 1, 2026