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Kohdent 6748

by Kohler Medizintechnik GmbH & Co. KG

Kohdent 6748 is a Class I device made by Kohler Medizintechnik GmbH & Co. KG, listed in FDA GUDID since 30 Aug 2021 (UDI-DI 04251436920998), 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 Number04251436920998 UDI-DI Date30 Aug 2021ListedStatusListed 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  • Withdrawn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
Kohdent
Generic name
Periotome, reusable
Model / Ref / Catalog
6748
Primary DI / UDI-DI
04251436920998
FDA product code
NDP
GMDN term
Periotome, reusable
Device class
Class I
Regulation number
872.3980
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Periotome, reusable

Other devices from Kohler Medizintechnik GmbH & Co. KG

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Properties

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