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Bite Impression Coping OBICR7002P

by POINTIMPLANT Co., Ltd.

Bite Impression Coping OBICR7002P is a Class I device made by POINTIMPLANT Co., Ltd., listed in FDA GUDID since 9 May 2025 (UDI-DI 08800011264277), 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 Number08800011264277 UDI-DI Date9 May 2025ListedStatusListed 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  • Withdrawn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 precision attachment simulator/analog, single-use
Model / reference
OBICR7002P
Primary DI / UDI-DI
08800011264277
FDA product code
NDP
GMDN term
Dental precision attachment simulator/analog, single-use
Device class
Class I
Regulation number
872.3980
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
MRI safety
MR Conditional

Related devices

Category: Dental precision attachment simulator/analog, single-use

Other devices from POINTIMPLANT Co., Ltd.

See all devices from POINTIMPLANT Co., Ltd. →

Properties

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