Dentronix, Inc. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
FDA 510(k) Regulatory Record - Dentronix, Inc. General & Plastic Surgery ✕
7 devices
Cleared
Jun 17, 1977
NEW PODIATRY PRODUCTS
General & Plastic Surgery
15d
Cleared
Jun 17, 1977
MODIFIED PODIATRY PRODUCTS
General & Plastic Surgery
15d
Cleared
Mar 09, 1977
CUTTER, P606 BONE
General & Plastic Surgery
21d
Cleared
Mar 09, 1977
NIPPER, NAIL, P610 ENGLISH
General & Plastic Surgery
21d
Cleared
Mar 09, 1977
CUTTER, P605 GENERAL PURPOSE
General & Plastic Surgery
21d
Cleared
Mar 09, 1977
CUTTER, P607 BONE
General & Plastic Surgery
21d
Cleared
Mar 07, 1977
NIPPER, PSO4 TISSUE
General & Plastic Surgery
19d