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Bone Compaction Drill BCD5005

by OSSTEM IMPLANT Co., Ltd. 2 variants

Bone Compaction Drill BCD5005 is a Class I device made by OSSTEM IMPLANT Co., Ltd., listed in FDA GUDID since 27 May 2024 (UDI-DI 08809917144126), 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 Number08809917144126 UDI-DI Date27 May 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  • Withdrawn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
Bone Compaction Drill
Generic name
Fixture/appliance dental drill bit, reusable
Model / reference
BCD5005
Primary DI / UDI-DI
08809917144126
FDA product code
DZA
GMDN term
Fixture/appliance dental drill bit, reusable
Device class
Class I
Regulation number
872.4130
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Fixture/appliance dental drill bit, reusable

Other devices from OSSTEM IMPLANT Co., Ltd.

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

Properties

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