# Osteometer Meditech A/S

- Location (FDA's records): Dallas, TX
- FDA decisions: 3 (1997–2000): 2 510(k) clearances and 1 original PMA approval
- Product codes: KGI (2), MUA (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (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 that cite its devices most
- Demetech Corp.: 1 (https://510kreport.com/company/demetech)
- Osteometer Meditech, Inc.: 1 (https://510kreport.com/company/osteometer-meditech)

## Its most-cited devices
- K964562: DTX-200 Bone Densitometer (1997), cited by 2

## Recent decisions
- P980010: Dtu-One Ultrasound Scanner (Sep 19, 2000)
- K964562: DTX-200 Bone Densitometer (Aug 22, 1997)
- K963789: DTX-100 Bone Densitometer (Jul 14, 1997)

Source page: https://510kreport.com/company/osteometer-meditech-a-s