Protean PRT-TDG-20

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	Number00841506150987 UDI-DI	Date11 Jun 2026Listed	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Withdrawn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: Surgical drill guide, reusable
Model / Ref / Catalog: PRT-TDG-20

Primary DI / UDI-DI: 00841506150987
FDA Product Code: LXH
GMDN Term: Surgical drill guide, reusable

Device Class: Class I
Regulation Number: 888.4540
GUDID distribution status: In Commercial Distribution

Sterilization Method: Moist Heat or Steam Sterilization

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Class II
GEMINUS Hook Plate, Radial, Left

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See all devices from Skeletal Dynamics L.L.C. →

Properties

Single Use
Prescription Use
Premarket Exempt
Lot / Batch Number

Other properties (10)

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