Thommen Medical AG
Thommen Medical AG holds FDA 510(k) medical device clearances, first cleared 2002, most recent 2017, with 2 FDA device recalls on record.
Top product codes for Thommen Medical AG
FDA recalls by Thommen Medical AG
- Z-1322-2024 — impression coping, repositionable, short, screw-retained, PF 4.0
- Z-1390-2019 — Adapter for handpiece, guided, reusable, for guide sleeve 0 4.8 mm Article number: 3.04.090 - Product Usage: The adapter for handpiece, guided reusable, for guide sleeve ¿ 4.8 mm is used to transfer the implant from the packaging to the patient via a plug-in connection and screwed in manually or mechanically.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Thommen Medical AG
- K171795 — Thommen Implant System
- K160244 — VARIOunite
- K151984 — Thommen Milling Abutment for CAD/CAM
- K121334 — VARIOECO
- K111984 — SPI VARIO ANGLED ABUTMENT
- K102804 — SPI TITANIUM BASE FOR CAD/CAM
- K101798 — SPI VARIOMULTI ANGLED ABUTMENT
- K093615 — SPI DENTAL IMPLANT, ELEMENT
- K092248 — SPI CUSTOMIZABLE GINGIVA FORMER
- K090154 — SPI DENTAL IMPLANT INICELL
- K090153 — SPI VARIOMULTI ANGLED ABUTMENT
- K072856 — SPI VARIOMULTI ABUTMENT
- K072649 — SPI SYSTEM DENTAL IMPLANTS
- K073141 — SPI ART ABUTMENT
- K072933 — SPI CONTACT PLATFORM O 4.0 MM
- K071453 — SPI EASY 4.0 ABUTMENT
- K070290 — SPI VECTODRILL CERAMIC DRILLS
- K070007 — SPI ELEMENT PLATFORM O 4.0 MM
- K061807 — SPI ART ABUTMENTS
- K051527 — SPI EASY TEMPORARY CAP
- K051502 — SPI DENTAL IMPLANT
- K034014 — SPI CONTACT DENTAL IMPLANT
- K033346 — SPI EASY DENTAL IMPLANT PROTECTIVE CAP
- K031747 — SPI DENTAL IMPLANT ABUTMENTS
- K030689 — SPI ELEMENT DENTAL IMPLANT O 3.5 MM
- K023645 — SPI EASY DENTAL IMPLANT ABUTMENT
Data sourced from openFDA. This site is unofficial and independent of the FDA.