# Miha Bodytec GmbH

- Location (FDA's records): Gersthofen, DE
- FDA decisions: 3 (2019–2022): 3 510(k) clearances
- Product codes: NGX (3)
- 510(k) review time since 2016: median 238 days, against 256 for FDA's reviews in the same codes and years (2 of 3 faster)
- Predicates its devices cite: 5 (2 its own); citations of its devices by later devices: 3 (2 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
- Chattanooga Group, Inc.: 1 (https://510kreport.com/company/chattanooga-group)
- Fit-Pro Kft, Ltd.: 1 (https://510kreport.com/company/fit-pro-kft)
- Katalyst, Inc.: 1 (https://510kreport.com/company/katalyst)

## Firms that cite its devices most
- Neuro20 Technologies: 1 (https://510kreport.com/company/neuro20-technologies)

## Its most-cited devices
- K201975: miha bodytec II (2021), cited by 2
- K182519: Miha Bodytec II (2019), cited by 1

## Recent decisions
- K221498: Miha Bodytec II (Oct 7, 2022)
- K201975: miha bodytec II (Mar 11, 2021)
- K182519: Miha Bodytec II (Jun 7, 2019)

Source page: https://510kreport.com/company/miha-bodytec