# Carticept Medical, Inc.

- Location (FDA's records): Alpharetta, GA
- FDA decisions: 6 (2011–2015): 6 510(k) clearances
- Product codes: FRN (6)
- Predicates its devices cite: 8 (5 its own); citations of its devices by later devices: 5 (5 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
- Milestone Scientific, Inc.: 1 (https://510kreport.com/company/milestone-scientific)
- Sonosite,Inc.: 1 (https://510kreport.com/company/sonosite)
- Hk Surgical, Inc.: 1 (https://510kreport.com/company/hk-surgical)

## Its most-cited devices
- K120830: Navigator Delivery System (Navigator DS) (2012), cited by 1
- K101194: Navigator Delivery System (or Navigator DS) Model: Nav-010 (2011), cited by 1
- K112067: Navigator Delivery System (Navigator DS) (2011), cited by 1
- K124053: Navigator Delivery System (Navigator DS) (2013), cited by 1
- K122215: Navigator Delivery System (Navigator DS) (2012), cited by 1

## Recent decisions
- K151255: Navigator Aesthetic Delivery System (Dec 30, 2015)
- K124053: Navigator Delivery System (Navigator DS) (Mar 13, 2013)
- K122215: Navigator Delivery System (Navigator DS) (Oct 26, 2012)
- K120830: Navigator Delivery System (Navigator DS) (Apr 16, 2012)
- K112067: Navigator Delivery System (Navigator DS) (Sep 16, 2011)
- K101194: Navigator Delivery System (or Navigator DS) Model: Nav-010 (Jul 11, 2011)

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