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Doctor Nice 113989

by B. Ali Impex

Doctor Nice 113989 is a Class I device made by B. Ali Impex, listed in FDA GUDID since 29 Jan 2024 (UDI-DI 08964003163631), 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 Number08964003163631 UDI-DI Date29 Jan 2024ListedStatusListed 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  • Withdrawn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
Doctor Nice
Generic name
Facebow
Model / reference
113989
Primary DI / UDI-DI
08964003163631
FDA product code
KTZ
GMDN term
Facebow
Device class
Class I
Regulation number
888.4150
GUDID distribution status
In Commercial Distribution

Related devices

Category: Facebow

Similar devices in this category

Other devices filed under Facebow.

Other devices from B. Ali Impex

See all devices from B. Ali Impex →

Properties

  • Sterilise before use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)