EIL — Gauge, Depth, Instrument, Dental Class I
FDA Device Classification
Classification Details
- Product Code
- EIL
- Device Class
- Class I
- Regulation Number
- 872.4565
- Submission Type
- Review Panel
- DE
- Medical Specialty
- Dental
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
| K911643 | abiomed | ABIODENT PERIOTEMP(R) SYSTEM | July 9, 1991 |
| K890493 | florida probe | FLORIDA PROBE PERIODONTAL PROBE | March 13, 1989 |
| K885075 | abiomed | ABIOMED PERIOTEMP(TM) PROBE | February 13, 1989 |
| K884813 | vine valley research | MODEL 200A ELECTRONIC FORCE-SENSING PROBE | January 5, 1989 |
| K880209 | dentsply intl | PERIODONTAL PROBE - AUTOPROBE | April 27, 1988 |
| K872098 | bowen and company | CREMEEN ALVEOLAR BONE CALIPER | July 31, 1987 |
| K872215 | bernard loewenthal | PERIO-TEST | July 10, 1987 |
| K822793 | national patent development | PIO ROOT CANAL INDICATOR | October 22, 1982 |