Cytophil, Inc.
Cytophil, Inc. appears in FDA public data with 0 recalls, 8 510(k) clearances, 5 FDA inspections, and 1 compliance action on record. Its most recent 510(k) clearance was granted on Apr 6, 2015.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 8
- Inspections
- 5
- Compliance Actions
- 1
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| 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 |
| K081815 | VOCALIS GEL | Jan 5, 2009 |
| K081816 | VOCALIS AND VOCALIS SM | Jan 5, 2009 |
| K072219 | CYTOPHIL TISSUE MARKER | Jan 18, 2008 |