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SABLE - Kavo Multiflex 2000105

by Sable Industries Inc

SABLE - Kavo Multiflex 2000105 is a Class I device made by Sable Industries Inc, cleared under FDA 510(k) K072554 on 14 Nov 2007 and listed in FDA GUDID since 25 Jul 2022 (UDI-DI 00841359050052), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

510(k) K072554

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00841359050052 UDI-DI Date25 Jul 2022ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Abbreviated NumberK072554 Date14 Nov 2007DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K072554 decided 14 Nov 2007 Active
  • FDA GUDID UDI-DI 00841359050052 listed 25 Jul 2022 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K072554
  2. Listed FDA GUDID 00841359050052

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name
SABLE - Kavo Multiflex
Generic name
Pneumatic dental handpiece coupler
Model / reference
2000105
Primary DI / UDI-DI
00841359050052
510(k) Number
FDA product code
EFB
GMDN term
Pneumatic dental handpiece coupler
Device class
Class I
Regulation number
872.4200
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code EFB (Handpiece, Air-Powered, Dental).

Other devices from Sable Industries Inc

See all devices from Sable Industries Inc →

Properties

  • Prescription use
  • Serial number
Other properties (13, all answered No)