# Restorative Therapies, Inc.

- Location (FDA's records): Baltimore, MD
- FDA decisions: 10 (2005–2017): 10 510(k) clearances
- Product codes: GZI (9), IPF (1)
- Predicates its devices cite: 15 (9 its own); citations of its devices by later devices: 11 (9 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
- Therapeutic Technologies, Inc.: 4 (https://510kreport.com/company/therapeutic-technologies)
- Danmeter A/S: 1 (https://510kreport.com/company/danmeter-a-s)
- Hasomed GmbH: 1 (https://510kreport.com/company/hasomed)

## Firms that cite its devices most
- Hasomed GmbH: 1 (https://510kreport.com/company/hasomed)
- Myolyn, LLC: 1 (https://510kreport.com/company/myolyn)

## Its most-cited devices
- K090750: RT300-SL, Model FA100052; RT300-Slsa, Model FA104581 (2009), cited by 4
- K060032: RT300-S, Model FA100052; RT300-SP, Model FA100053 (2006), cited by 2
- K072398: RT300-S and RT300-SP Fes Cycle Ergometer (2007), cited by 1
- K071486: RT300-S, RT300-SP (Pediatric Version), Model FA100052, FA100053 (2007), cited by 1
- K071113: RT300-S, Model FA100052, RT300-SP (Pediatric Version), Model FA100053 (2007), cited by 1
- K160614: Xcite Clinical Station (2016), cited by 1

## Recent decisions
- K162470: RT300 FES cycle ergometer (Jul 11, 2017)
- K160614: Xcite Clinical Station (Dec 16, 2016)
- K103370: RT200 (Apr 5, 2011)
- K103366: RT600 (Apr 4, 2011)
- K090750: RT300-SL, Model FA100052; RT300-Slsa, Model FA104581 (Aug 5, 2009)
- K072398: RT300-S and RT300-SP Fes Cycle Ergometer (Nov 21, 2007)
- K071486: RT300-S, RT300-SP (Pediatric Version), Model FA100052, FA100053 (Sep 10, 2007)
- K071113: RT300-S, Model FA100052, RT300-SP (Pediatric Version), Model FA100053 (Jul 5, 2007)

Source page: https://510kreport.com/company/restorative-therapies