Product code DZM— Dental
ASEPTIC DENTAL TECH. TOTAL TREATMENT SYSTEM
- Classification name
- Needle, Dental
- Device class
- Class 1
- Regulation
- 21 CFR 872.4730
- Advisory panel
- Dental
- Total cleared
- 16
- First cleared
- Most recent
Market context for product code DZM
FDA has cleared devices under product code DZM between 1976 and 1999, filed by 14 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
- 1992
- 1991
- 1990
- 1989
- 1987
- 1986
- 1985
- 1984
- 1982
- 1980
- 1976
Top applicants under product code DZM
Adverse events under product code DZM
product code DZM- Injury
- 139
- Total
- 139
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Recent clearances under product code DZM
- K990511 — X-TIP INTRAOSSEOUS PERFORATOR
- K920758 — JENKER NEEDLE STICK PROTECTOR
- K914562 — ASEPTIC DENTAL TECH. TOTAL TREATMENT SYSTEM
- K913573 — SAFETY PLUS DENTAL INJECTION NEEDLE
- K910475 — DENTAL NEEDLE PROTECTIVE SYSTEM
- K910446 — STABIDENT LOCAL ANESTHESIA SYSTEM
- K896219 — SAFE-T-CAP NEEDLE COVER
- K894373 — NIPRO DENTAL NEEDLE
- K870921 — DENTAL NEEDLE (CARTRIDGE TYPE)
- K864970 — TERUMO DENTAL NEEDLES
- K861150 — EXEL DENTAL NEEDLE
- K851524 — SEPTOJECT STERILE DISPOSABLE INJECTION NEEDLE
- K833304 — HYPO BRAND DISPOS. DENTAL NEEDLES-PLAST
- K820568 — MUSCLE DYSFUNCTION MONITOR
- K802811 — MONOJECT ROOT CANAL FILLING MAT. NEEDLE
- K761206 — INTEROSSEOUS NEEDLE
Data sourced from openFDA. This site is unofficial and independent of the FDA.