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9185 Facebow

by Whip-Mix Corp.

9185 Facebow is a Class I device made by Whip-Mix Corp., listed in FDA GUDID since 22 Sep 2020 (UDI-DI D040341261), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberD040341261 UDI-DI Date22 Sep 2020ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Generic name
Facebow
Model / Ref / Catalog
9185
Primary DI / UDI-DI
D040341261
FDA product code
KCR
GMDN term
Facebow
Device class
Class I
Regulation number
872.3220
GUDID distribution status
In Commercial Distribution

Related devices

Category: Facebow

Similar devices in this category

Other devices filed under Facebow.

Other devices from Whip-Mix Corp.

See all devices from Whip-Mix Corp. →

Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)