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Klockner 90 14 01

by Soadco, S.L.

Klockner 90 14 01 is a Class II device made by Soadco, S.L., cleared under FDA 510(k) K080224 on 3 Jul 2008 and listed in FDA GUDID since 14 Feb 2025 (UDI-DI 08435451610737), 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) K080224

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 Number08435451610737 UDI-DI Date14 Feb 2025ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK080224 Date3 Jul 2008DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K080224 decided 3 Jul 2008 Active
  • FDA GUDID UDI-DI 08435451610737 listed 14 Feb 2025 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K080224
  2. Listed FDA GUDID 08435451610737

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Klockner
Generic name
Overdenture
Model / Ref / Catalog
90 14 01
Primary DI / UDI-DI
08435451610737
510(k) Number
FDA product code
NHA
GMDN term
Overdenture
Device class
Class II
Regulation number
872.3630
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Similar devices

Other devices filed under FDA product code NHA (Abutment, implant, dental, endosseous).

Other devices from Soadco, S.L.

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Properties

  • Sterilise before use
  • Single use
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)