Sharpoint, Inc.
Sharpoint, Inc. appears in FDA public data with 0 recalls, 9 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on October 24, 1986.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 9
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K863595 | COATED SUTURE NEEDLE | October 24, 1986 |
| K861947 | SURGICAL KNIFE | June 6, 1986 |
| K840764 | EAR KNIVES | May 21, 1984 |
| K840855 | CORNEAL SCLERAL LANCE | May 9, 1984 |
| K840660 | POSTERIOR CAPSULOTOMY CYSTITOME | March 16, 1984 |
| K840659 | ANTERIOR CAPSULECTOMY CYSTITOME | March 16, 1984 |
| K830522 | STAINLESS STEEL SUTURE 316L | March 31, 1983 |
| K822112 | OPHTHALMIC KNIFE | August 10, 1982 |
| K821440 | V LANCE | June 14, 1982 |