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PWX736

by G&H Wire Company, Inc.

PWX736 is a Class I device made by G&H Wire Company, Inc., listed in FDA GUDID since 9 Oct 2023 (UDI-DI 10190886106303), 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 Number10190886106303 UDI-DI Date9 Oct 2023ListedStatusListed 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  • Withdrawn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

Generic name
Orthodontic appliance relief material
Model / reference
PWX736
Primary DI / UDI-DI
10190886106303
FDA product code
EGD
GMDN term
Orthodontic appliance relief material
Device class
Class I
Regulation number
872.6890
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code EGD (Wax, Dental, Intraoral).

Other devices from G&H Wire Company, Inc.

See all devices from G&H Wire Company, Inc. →

Properties

  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)