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Dyna Locking Trochanteric Nail NG3013

by CG MedTech Co., Ltd.

Dyna Locking Trochanteric Nail NG3013 is a Class I device made by CG MedTech Co., Ltd., listed in FDA GUDID since 31 Oct 2017 (UDI-DI 08800015948913), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08800015948913 UDI-DI Date31 Oct 2017ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Dyna Locking Trochanteric Nail
Generic name
Orthopaedic implant driver
Model / reference
NG3013
Primary DI / UDI-DI
08800015948913
FDA product code
HXX
GMDN term
Orthopaedic implant driver
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Orthopaedic implant driver

Similar devices in this category

Other devices filed under Orthopaedic implant driver.

Other devices from CG MedTech Co., Ltd.

See all devices from CG MedTech Co., Ltd. →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Serial number
Other properties (10, all answered No)