Skip to content

Zibone Me-D4822

by Coho Biomedical Technology Co., Ltd.

Zibone Me-D4822 is a dental power tool converter attachment (FDA Class I; FDA product code NDP, Accessories, Implant, Dental, Endosseous) made by Coho Biomedical Technology Co., Ltd., listed in FDA GUDID since 1 May 2020 (UDI-DI 04710986432622), 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 Number04710986432622 UDI-DI Date1 May 2020ListedStatusListed 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  • Withdrawn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
Zibone
Generic name
Dental power tool converter attachment, rotary
Model / reference
Me-D4822
Primary DI / UDI-DI
04710986432622
FDA product code
NDP
GMDN term
Dental power tool converter attachment, rotary
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 power tool converter attachment, rotary

Similar devices

Other devices filed under FDA product code NDP (Accessories, Implant, Dental, Endosseous).

Other devices from Coho Biomedical Technology Co., Ltd.

See all devices from Coho Biomedical Technology Co., Ltd. →

Properties

  • Sterilise before use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)