Dentronix, Inc.
Dentronix, Inc. has 0 FDA recalls, 0 inspections, 9 510(k) clearances and 0 compliance actions on record.
- Latest 510(k)
- Mar 13, 1991
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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 | 9 | Nov 8, 2026 | File dated Nov 2, 2026 | Current |
| Inspections | 0 | Nov 14, 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 |
|---|---|---|
| K910202 | DENTRONIX MODEL 2000 | Mar 13, 1991 |
| K880322 | DENTRONIX DDS 5000 DRY HEAT STERILIZATION SYSTEM | Jul 13, 1988 |
| K771005 | NEW PODIATRY PRODUCTS | Jun 17, 1977 |
| K771006 | MODIFIED PODIATRY PRODUCTS | Jun 17, 1977 |
| K770302 | CUTTER, P606 BONE | Mar 9, 1977 |
| K770305 | CUTTER, P607 BONE | Mar 9, 1977 |
| K770304 | CUTTER, P605 GENERAL PURPOSE | Mar 9, 1977 |
| K770303 | NIPPER, NAIL, P610 ENGLISH | Mar 9, 1977 |
| K770301 | NIPPER, PSO4 TISSUE | Mar 7, 1977 |
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