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Dentronix, Inc.

FDA 510(k) & PMA Approved Devices — 9 products

Total Devices9
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K910202 DENTRONIX MODEL 2000KMH1991-03-13 View
510(k) K880322 DENTRONIX DDS 5000 DRY HEAT STERILIZATION SYSTEMKMH1988-07-13 View
510(k) K771006 MODIFIED PODIATRY PRODUCTSHTZ1977-06-17 View
510(k) K771005 NEW PODIATRY PRODUCTSHTZ1977-06-17 View
510(k) K770305 CUTTER, P607 BONEFZT1977-03-09 View
510(k) K770302 CUTTER, P606 BONEFZT1977-03-09 View
510(k) K770303 NIPPER, NAIL, P610 ENGLISHFZT1977-03-09 View
510(k) K770304 CUTTER, P605 GENERAL PURPOSEFZT1977-03-09 View
510(k) K770301 NIPPER, PSO4 TISSUEFZT1977-03-07 View
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