# Cymedica Orthopedics, Inc.

- Location (FDA's records): Scottsdale, AZ
- FDA decisions: 5 (2015–2023): 5 510(k) clearances
- Product codes: IPF (4), GXY (1)
- 510(k) review time since 2016: median 44 days, against 111 for FDA's reviews in the same codes and years (4 of 4 faster)
- Predicates its devices cite: 7 (3 its own); citations of its devices by later devices: 5 (3 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
- Bio-Medical Research, Ltd.: 2 (https://510kreport.com/company/bio-medical-research)
- Umeheal, Ltd.: 1 (https://510kreport.com/company/umeheal)
- Neurometrix, Inc.: 1 (https://510kreport.com/company/neurometrix)

## Firms that cite its devices most
- Timewaver Production GmbH: 1 (https://510kreport.com/company/timewaver-production)
- Ncs Lab Srl: 1 (https://510kreport.com/company/ncs-lab)

## Its most-cited devices
- K163067: CyMedica e-vive™ System; CY-1000 (2016), cited by 2
- K150413: QB1 System Powered Muscle Stimulator & Transcutaneous Electrical Nerve Stimulator (2015), cited by 2
- K210604: Intellihab System (2021), cited by 1

## Recent decisions
- K230533: Motive™ Electrode (Mar 22, 2023)
- K220738: Motive Knee Wrap (May 12, 2022)
- K210604: Intellihab System (Jun 3, 2021)
- K163067: CyMedica e-vive™ System; CY-1000 (Dec 1, 2016)
- K150413: QB1 System Powered Muscle Stimulator & Transcutaneous Electrical Nerve Stimulator (Apr 2, 2015)

Source page: https://510kreport.com/company/cymedica-orthopedics