Surgidev Corp.
Surgidev Corp. has 0 FDA recalls, 0 inspections, 4 510(k) clearances and 0 compliance actions on record.
- Latest 510(k)
- Apr 9, 1985
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Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Nov 8, 2026 | File dated Nov 3, 2026 | Current |
| 510(k) clearances | 4 | Nov 8, 2026 | File dated Nov 2, 2026 | Current |
| Inspections | 0 | Nov 13, 2026 | Newest record Nov 5, 2026 | Current |
| Compliance actions | 0 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
Recent 510(k) clearances
| K-Number | Device | Date |
|---|---|---|
| K850729 | ACUFLO VOLUMETRIC CONTROLLED DELIVERY SYS 2000 | Apr 9, 1985 |
| K831829 | KARICKHOFF FLYING CORPUSCLE VIEWER | Oct 19, 1983 |
| K831975 | LEADING EDGE OPHTHALMIC KNIFE | Aug 31, 1983 |
| K830008 | KARICKHOFF KERATOSCOPE | Jan 26, 1983 |
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