Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in SwitzerlandLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Storz Medical AG with 3 510(k) clearances. The most recent is a 510(k) clearance dated May 3, 2021: Storz Medical MAGNETOLITH Muscle Stimulator.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| May 3, 2021 | Storz Medical MAGNETOLITH Muscle StimulatorK203710 · IPF | 510(k) clearances |
| Feb 21, 2021 | Storz Medical Duolith SD1 T-Top & Tower System with C-Actor Sepia HandpieceK202112 · PZL | 510(k) clearances |
| Apr 13, 2018 | D-Actor 200 Vibration Massage SystemK173692 · ISA | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
