Company ยท US
Dentronix, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1977 to 1991. Name variants (Inc, Corp, punctuation) are merged.
9510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Mar 13, 1991 | K910202 | DENTRONIX MODEL 2000 Dentronix, Inc. | KMH |
| Jul 13, 1988 | K880322 | DENTRONIX DDS 5000 DRY HEAT STERILIZATION SYSTEM Dentronix, Inc. | KMH |
| Jun 17, 1977 | K771006 | MODIFIED PODIATRY PRODUCTS Dentronix, Inc. | HTZ |
| Jun 17, 1977 | K771005 | NEW PODIATRY PRODUCTS Dentronix, Inc. | HTZ |
| Mar 9, 1977 | K770305 | CUTTER, P607 BONE Dentronix, Inc. | FZT |
| Mar 9, 1977 | K770304 | CUTTER, P605 GENERAL PURPOSE Dentronix, Inc. | FZT |
| Mar 9, 1977 | K770303 | NIPPER, NAIL, P610 ENGLISH Dentronix, Inc. | FZT |
| Mar 9, 1977 | K770302 | CUTTER, P606 BONE Dentronix, Inc. | FZT |
| Mar 7, 1977 | K770301 | NIPPER, PSO4 TISSUE Dentronix, Inc. | FZT |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||