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Imtec Im-Bnc-1

by Park Dental Research Corp

Imtec Im-Bnc-1 is a Class I device made by Park Dental Research Corp, listed in FDA GUDID since 20 Aug 2024 (UDI-DI D769IMBNC10), 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 NumberD769IMBNC10 UDI-DI Date20 Aug 2024ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Imtec
Generic name
Facebow
Model / Ref / Catalog
IM-BNC-1, BNC-1
Primary DI / UDI-DI
D769IMBNC10
FDA product code
NDP
GMDN term
Facebow
Device class
Class I
Regulation number
872.3980
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Facebow

Similar devices in this category

Other devices filed under Facebow.

Other devices from Park Dental Research Corp

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Properties

  • Sterilise before use
  • Prescription use
  • Lot / batch number
Other properties (12, all answered No)