# Cytophil, Inc.

- Location (FDA's records): East Troy, WI
- FDA decisions: 8 (2008–2015): 8 510(k) clearances
- Product codes: MIX (4), LYC (2), MQV (1), NEU (1)
- Predicates its devices cite: 15 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Coapt Systems, Inc.: 4 (https://510kreport.com/company/coapt-systems)
- Bioform, Inc.: 3 (https://510kreport.com/company/bioform)
- Bioform Medical, Inc.: 3 (https://510kreport.com/company/bioform-medical)
- Biomatlante: 2 (https://510kreport.com/company/biomatlante)
- Cam Implants B.V.: 1 (https://510kreport.com/company/cam-implants)
- Septodont, Inc.: 1 (https://510kreport.com/company/septodont)
- Medtronic Sofamor Danek: 1 (https://510kreport.com/company/medtronic-sofamor-danek)

## Firms that cite its devices most
- Kent Medical Devices, Inc.: 1 (https://510kreport.com/company/kent-medical-devices)

## Its most-cited devices
- K072219: Cytophil Tissue Marker (2008), cited by 1

## Recent decisions
- K150400: Renu Gel (Apr 6, 2015)
- K121795: Calcium Hydroxylapatite Vocal Fold Implant (Feb 22, 2013)
- K102937: Osteophil Beta-TCP (Dec 27, 2010)
- K093871: Periophil B-TCP (Apr 22, 2010)
- K092788: Periophil Biphasic (Dec 18, 2009)
- K081816: Vocalis and Vocalis SM (Jan 5, 2009)
- K081815: Vocalis Gel (Jan 5, 2009)
- K072219: Cytophil Tissue Marker (Jan 18, 2008)

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