# Arm Medical Devices, Inc.

- Location (FDA's records): Bristol, CT
- FDA decisions: 1 (2010–2010): 1 510(k) clearance
- Product codes: BSK (1)
- Predicates its devices cite: 5 (0 its own); citations of its devices by later devices: 5 (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
- Diemolding Corp.: 1 (https://510kreport.com/company/diemolding)
- Posey Co.: 1 (https://510kreport.com/company/posey)
- Rusch Intl.: 1 (https://510kreport.com/company/rusch-intl)
- Extracorporeal Medical Specialities, Inc.: 1 (https://510kreport.com/company/extracorporeal-medical-specialities)
- Sunmed, Inc.: 1 (https://510kreport.com/company/sunmed)

## Firms that cite its devices most
- Hamilton Medical AG: 2 (https://510kreport.com/company/hamilton-medical)
- Hospitech Respiration, Ltd.: 2 (https://510kreport.com/company/hospitech-respiration)
- Venner Medical (Singapore) Pte, Ltd.: 1 (https://510kreport.com/company/venner-medical-singapore)

## Its most-cited devices
- K092733: PYTON (2010), cited by 5

## Recent decisions
- K092733: PYTON (Feb 26, 2010)

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