# Storz Medical AG

- Location (FDA's records): Tagerwilen, CH
- FDA decisions: 4 (2016–2021): 3 510(k) clearances and 1 original PMA approval
- Product codes: NBN (1), IPF (1), ISA (1), PZL (1)
- Predicates its devices cite: 6 (0 its own); citations of its devices by later devices: 8 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Asclepion Laser Technologies GmbH: 2 (https://510kreport.com/company/asclepion-laser-technologies)
- BTL Industries, Inc.: 1 (https://510kreport.com/company/btl-industries)
- Bemer Int AG: 1 (https://510kreport.com/company/bemer-int)
- Sanuwave, Inc.: 1 (https://510kreport.com/company/sanuwave)
- Tissue Regeneration Technologies, LLC: 1 (https://510kreport.com/company/tissue-regeneration-technologies)

## Firms that cite its devices most
- E.M.S Electro Medical Systems S.A: 2 (https://510kreport.com/company/ems-electro-medical-systems-s-a)
- BTL Industries, Inc.: 2 (https://510kreport.com/company/btl-industries)
- Tissue Regeneration Technologies, LLC: 1 (https://510kreport.com/company/tissue-regeneration-technologies)
- Medispec, Ltd.: 1 (https://510kreport.com/company/medispec)
- Termosalud: 1 (https://510kreport.com/company/termosalud)
- Quantumtx Pte., Ltd.: 1 (https://510kreport.com/company/quantumtx)

## Its most-cited devices
- K173692: D-Actor 200 Vibration Massage System (2018), cited by 5
- K203710: Storz Medical MAGNETOLITH Muscle Stimulator (2021), cited by 2
- K202112: Storz Medical Duolith SD1 T-Top & Tower System with C-Actor Sepia Handpiece (2021), cited by 1

## Recent decisions
- K203710: Storz Medical MAGNETOLITH Muscle Stimulator (May 3, 2021)
- K202112: Storz Medical Duolith SD1 T-Top & Tower System with C-Actor Sepia Handpiece (Feb 21, 2021)
- K173692: D-Actor 200 Vibration Massage System (Apr 13, 2018)
- P080028: Storz Medical Duolith SD1 Shock Wave Therapy (Jan 8, 2016)

Source page: https://510kreport.com/company/storz-medical