# Medrobotics Corporation

- Location (FDA's records): Raynham, MA
- FDA decisions: 5 (2015–2018): 5 510(k) clearances
- Product codes: FDF (2), EOB (2), HET (1)
- 510(k) review time since 2016: median 246 days, against 36 for FDA's reviews in the same codes and years (1 of 3 faster)
- Predicates its devices cite: 8 (2 its own); citations of its devices by later devices: 2 (2 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Neoguide Systems, Inc.: 3 (https://510kreport.com/company/neoguide-systems)
- Vision-Sciences, Inc.: 2 (https://510kreport.com/company/vision-sciences)
- Olympus Medical Systems Corp.: 1 (https://510kreport.com/company/olympus-medical-systems)

## Its most-cited devices
- K162330: Flex Robotic System and Flex Colorectal Drive (2017), cited by 1
- K150776: Medrobotics Flex System (2015), cited by 1

## Recent decisions
- K172796: Flex Robotic System and Flex Transabdominal Drive (Jan 18, 2018)
- K170453: Medrobotics Flex Robotic System (Oct 19, 2017)
- K172036: Medrobotics Flex Robotic System (Aug 3, 2017)
- K162330: Flex Robotic System and Flex Colorectal Drive (May 4, 2017)
- K150776: Medrobotics Flex System (Jul 17, 2015)

Source page: https://510kreport.com/company/medrobotics