PROTEAN Fragment Hand Plating 2.0 Module

by Skeletal Dynamics L.L.C. GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 29 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00841506138220 UDI-DI	Date1 Dec 2025Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

GUDID

Trade Name: Protean
Generic Name: Device sterilization/disinfection container, reusable
Model / Ref / Catalog: PROTEAN Fragment Hand Plating 2.0 Module, PRT-HP-MOD20

Primary DI / UDI-DI: 00841506138220
510(k) Number: K102103
FDA Product Code: KCT
GMDN Term: Device sterilization/disinfection container, reusable

Device Class: Class II
Regulation Number: 880.6850
GUDID distribution status: In Commercial Distribution

Sterilization Method: Moist Heat or Steam Sterilization

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GEMINUS Hook Plate, Radial, Left

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Properties

Prescription Use
Lot / Batch Number

Other properties (12)

Sterile: No
Single Use: No
Implantable: No
Contains Latex: No
Over-the-Counter: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Premarket Exempt: No
Serial Number: No
Expiration Date: No
Manufacturing Date: No