Product code DZA— Dental
ADA SHANK EXTENSION
- Classification name
- Drill, Dental, Intraoral
- Device class
- Class 1
- Regulation
- 21 CFR 872.4130
- Advisory panel
- Dental
- Total cleared
- 13
- First cleared
- Most recent
Market context for product code DZA
FDA has cleared devices under product code DZA between 1976 and 1999, filed by 12 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
- 1999
- 1996
- 1993
- 1991
- 1990
- 1988
- 1981
- 1980
- 1976
Top applicants under product code DZA
Recent clearances under product code DZA
- K984508 — SURGICAL CONTRA-ANGLE HANDPIECES, MODELS 975 AE,979 E/KM, 985 AE, 986 AE, 988 E/KM AND SURGICAL STRAIGHT HANDPIECES MOD
- K962979 — S-53 INTRORAL DENTAL SYSTEM
- K954790 — PROFILE NICKEL TITANIUM ROTARY INSTRUMENTS
- K914724 — ADA SHANK EXTENSION
- K905418 — GATES GLIDDEN DRILLS
- K901097 — FILLOCK REAMER
- K896149 — ANEST-EZE DENTAL DRILL RA#2
- K884187 — INDENTEC DRILL RA #1
- K811113 — RIESS-LUHR
- K801887 — DRILL, DENTAL
- K801888 — HANDPIECE, DENTAL
- K761275 — AIROTOS LF HANDPIECE
- K760956 — SURGICAL MICRO DRILL
Data sourced from openFDA. This site is unofficial and independent of the FDA.