Product code DZH— Dental
ADD LINE DEVICES(PARTS) ELECTRIC HANDPIECE SYSTEMS
- Classification name
- Saw, Bone, Ac-Powered
- Device class
- Class 2
- Regulation
- 21 CFR 872.4120
- Advisory panel
- Dental
- Total cleared
- 4
- First cleared
- Most recent
Market context for product code DZH
FDA has cleared devices under product code DZH between 1976 and 2003, filed by 3 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.
Clearances per year
- 2003
- 1994
- 1976
Top applicants under product code DZH
Recent clearances under product code DZH
Data sourced from openFDA. This site is unofficial and independent of the FDA.