EIL
8 FDA 510(k) clearances · Product code
60 daysmedian time to decision
103 days90th percentile
8clearances measured
FDA profile
- Official device name
- Gauge, Depth, Instrument, Dental
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 872.4565
- Medical specialty
- Dental
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| ABIODENT PERIOTEMP(R) SYSTEM (K911643) | Abiomed, Inc. | 1991-07-09 |
| FLORIDA PROBE PERIODONTAL PROBE (K890493) | Florida Probe Corp. | 1989-03-13 |
| ABIOMED PERIOTEMP(TM) PROBE (K885075) | Abiomed, Inc. | 1989-02-13 |
| MODEL 200A ELECTRONIC FORCE-SENSING PROBE (K884813) | Vine Valley Research | 1989-01-05 |
| PERIODONTAL PROBE - AUTOPROBE (K880209) | Dentsply Intl. | 1988-04-27 |
| CREMEEN ALVEOLAR BONE CALIPER (K872098) | Bowen & Company, Inc. | 1987-07-31 |
| PERIO-TEST (K872215) | Dr. Bernard Loewenthal | 1987-07-10 |
| PIO ROOT CANAL INDICATOR (K822793) | National Patent Development Corp. | 1982-10-22 |
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Every clearance here is in the API, with alerts when new ones post.