# Clear Guide Medical

- Location (FDA's records): Baltimore, MD
- FDA decisions: 6 (2014–2024): 6 510(k) clearances
- Product codes: JAK (5), IYO (1)
- 510(k) review time since 2016: median 122 days, against 112 for FDA's reviews in the same codes and years (3 of 5 faster)
- Predicates its devices cite: 6 (4 its own); citations of its devices by later devices: 6 (4 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
- Philips Health Care: 1 (https://510kreport.com/company/philips-health-care)
- Inneroptic Technology, Inc.: 1 (https://510kreport.com/company/inneroptic-technology)

## Firms that cite its devices most
- Navifus Corporation: 1 (https://510kreport.com/company/navifus)
- Weipeng (Suzhou) Medical Devices Co., Ltd.: 1 (https://510kreport.com/company/weipeng-suzhou-medical-devices)

## Its most-cited devices
- K141806: Clear Guide One (2014), cited by 2
- K171677: Clear Guide SCENERGY (2017), cited by 2
- K153004: Clear Guide SCENERGY (2016), cited by 1
- K201188: Clear Guide SCENERGY (2020), cited by 1

## Recent decisions
- K234030: Clear Guide SCENERGY (Jan 17, 2024)
- K201188: Clear Guide SCENERGY (Sep 30, 2020)
- K201898: Clear Guide SCENERGY (Jul 31, 2020)
- K171677: Clear Guide SCENERGY (Dec 8, 2017)
- K153004: Clear Guide SCENERGY (Feb 12, 2016)
- K141806: Clear Guide One (Sep 19, 2014)

Source page: https://510kreport.com/company/clear-guide-medical