# Beam-Med, Ltd.

- Location (FDA's records): Petach Tikva, IL
- FDA decisions: 2 (2000–2011): 1 510(k) clearance and 1 original PMA approval
- Product codes: MUA (2)
- Predicates its devices cite: 1 (1 its own); citations of its devices by later devices: 3 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Echolight S.P.A: 1 (https://510kreport.com/company/echolight)
- Bone Index Finland, Ltd.: 1 (https://510kreport.com/company/bone-index-finland)

## Its most-cited devices
- K110646: Beammed Sunlight Miniomni Bone Sonometer (2011), cited by 2
- P990035: The Sunlight Omnisense (TM) Ultrasound Bone Sonometer (2000), cited by 1

## Recent decisions
- K110646: Beammed Sunlight Miniomni Bone Sonometer (Oct 12, 2011)
- P990035: The Sunlight Omnisense (TM) Ultrasound Bone Sonometer (Jan 20, 2000)

Source page: https://510kreport.com/company/beam-med