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WishFIX

FDA UDI

Class II (US FDA UDI)

by Wishbone Medical Inc.

Identity

Trade Name
WishFIX FDA UDI
Generic Name
Orthopaedic fixation plate, non-bioabsorbable FDA UDI
Device Name
Procedure Kit, Curved 4-Hole X 22mm WishFIX Plate, Instruments and Solid Screws, SS FDA UDI
Model / Reference
PK-EFC0422SS-08 FDA UDI
Description
Procedure Kit, Curved 4-Hole X 22mm WishFIX Plate, Instruments and Solid Screws, SS FDA UDI

Identifiers

Catalog Number
PK-EFC0422SS FDA UDI
Primary DI / UDI-DI
B562PKEFC0422SS080 FDA UDI
510(k) Number
K182704 FDA UDI
FDA Product Code
OBT FDA UDI
GMDN Term
Orthopaedic fixation plate, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 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

Yes

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

Yes

FDA UDI

Category: Orthopaedic fixation plate, non-bioabsorbable

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

Similar devices

Also classified as Orthopaedic fixation plate, non-bioabsorbable.

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 598cec56-f8c1-495c-8810-d8b91043ef7e 35 fields · synced May 30, 2026