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Bite Impression Coping BICRR4044S

by Izenimplant Co., Ltd.

Bite Impression Coping BICRR4044S is a Class I device made by Izenimplant Co., Ltd., listed in FDA GUDID since 11 Jun 2024 (UDI-DI 08800070236598), 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 Number08800070236598 UDI-DI Date11 Jun 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  • Withdrawn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
Bite Impression Coping
Generic name
Dental prosthesis/implant abutment screw analog, single-use
Model / reference
BICRR4044S
Primary DI / UDI-DI
08800070236598
FDA product code
NDP
GMDN term
Dental prosthesis/implant abutment screw analog, single-use
Device class
Class I
Regulation number
872.3980
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Dental prosthesis/implant abutment screw analog, single-use

Other devices from Izenimplant Co., Ltd

See all devices from Izenimplant Co., Ltd →

Properties

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