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US Fixture Transfer Impression Coping ICPM402S

by OSSTEM IMPLANT Co., Ltd.

US Fixture Transfer Impression Coping ICPM402S is a Class I device made by OSSTEM IMPLANT Co., Ltd., listed in FDA GUDID since 8 Dec 2022 (UDI-DI 08800040621270), 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 Number08800040621270 UDI-DI Date8 Dec 2022ListedStatusListed 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  • Withdrawn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
US Fixture Transfer Impression Coping
Generic name
Dental implant suprastructure, temporary, preformed, single-use
Model / reference
ICPM402S
Primary DI / UDI-DI
08800040621270
FDA product code
NDP
GMDN term
Dental implant suprastructure, temporary, preformed, 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 implant suprastructure, temporary, preformed, single-use

Other devices from OSSTEM IMPLANT Co., Ltd.

See all devices from OSSTEM IMPLANT Co., Ltd. →

Properties

  • Sterilise before use
  • Single use
  • Implantable
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Serial number
  • Manufacturing date
Other properties (7, all answered No)