Product code DZP— Dental
DIAMOND STONES
- Classification name
- Instrument, Diamond, Dental
- Device class
- Class 1
- Regulation
- 21 CFR 872.4535
- Advisory panel
- Dental
- Total cleared
- 21
- First cleared
- Most recent
Market context for product code DZP
FDA has cleared devices under product code DZP between 1976 and 2012, filed by 16 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.
Clearances per year
- 2012
- 1994
- 1993
- 1992
- 1990
- 1989
- 1988
- 1987
- 1985
- 1983
- 1980
- 1978
- 1976
Top applicants under product code DZP
Recent clearances under product code DZP
- K120037 — BLUWHITE DIAMOND DENTAL BURS MODIFIED
- K943841 — SOPHOS DENTAL DIAMOND
- K940908 — DUNHALL/OMNII INTERNATIONAL ROTARY DIAMOND BURS
- K934981 — DENTAL DRILL
- K923757 — DENTAL DIAMOND DRILLS
- K913651 — MANI DIA-BURS
- K901967 — DENDIA WERK BURS AND CUTTING DISCS
- K901262 — F.G. LASER (DENTAL BUR)
- K900089 — FG DIAMOND BURRS
- K893844 — 3D DENTAL DIAMOND ROTARY INSTRUMENTS
- K885233 — NOVA DIAMOND
- K880179 — BEAVERS' DENTAL DIAMOND INSTRUMENTS
- K871639 — DENTAL DIAMOND BURS
- K854347 — HYBRID POINTS
- K832856 — GINGI CURETTAGE DIAMOND POINTS
- K833038 — SUMMA DISK
- K832855 — TPE DIAMOND POINTS
- K802984 — MEISINGER DIAMOND DENTAL BURS
- K802987 — JOTA DIAMOND DENTAL BURS
- K780864 — DIAMOND STONES
- K760987 — DIAMOND STONES
Data sourced from openFDA. This site is unofficial and independent of the FDA.