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Klockner 90 14 08

by Soadco, S.L.

Klockner 90 14 08 is a Class II device made by Soadco, S.L., listed in FDA GUDID since 14 Feb 2025 (UDI-DI 08435451610782), 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 Number08435451610782 UDI-DI Date14 Feb 2025ListedStatusListed 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  • Withdrawn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
Klockner
Generic name
Overdenture
Model / Ref / Catalog
90 14 08
Primary DI / UDI-DI
08435451610782
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

Related devices

Category: Overdenture

Similar devices

Also classified as Overdenture.

Similar devices

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

Other devices from Soadco, S.L.

See all devices from Soadco, S.L. →

Properties

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