← Back to catalogue

Hook Plates

FDA UDI

Class II (US FDA UDI)

by Trimed, INC.

Identity

Trade Name
Hook Plates FDA UDI
Generic Name
Orthopaedic fixation plate, non-bioabsorbable FDA UDI
Device Name
Dorsal Wrist Hook Plate, 6-Hole FDA UDI
Model / Reference
WHKD-6 FDA UDI
Description
Dorsal Wrist Hook Plate, 6-Hole FDA UDI

Identifiers

Catalog Number
WHKD-6 FDA UDI
Primary DI / UDI-DI
00842188125331 FDA UDI
510(k) Number
K222637 FDA UDI
FDA Product Code
HRS 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

No

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic fixation plate, non-bioabsorbable

Hook Plates by Trimed, 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Trimed, INC.

Sources (1)

  • FDA UDI bdc05d70-3595-4421-b227-97561624c441 36 fields · synced May 30, 2026