Koi, Inc.
Koi, Inc. appears in FDA public data with 0 recalls, 7 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on April 30, 1986.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K843247 | KOI PACHYMETER | April 30, 1986 |
| K830366 | DIAMOND KNIFE | March 9, 1983 |
| K812764 | KOI BLUE FIELD ENTOPTOSCOPE | December 2, 1981 |
| K812450 | KOI DIAMOND KNIFE | September 21, 1981 |
| K812097 | KOI LACREMAL HOOK & DILATOR | August 18, 1981 |
| K812010 | KOI LACRIMAL INTUBATION SYSTEM | July 28, 1981 |
| K812011 | BLADE GAUGE | July 28, 1981 |