# Unit, Electrosurgical, And Accessories, Dental
> **Product code: EKZ** · Class II — Moderate Risk (510(k) clearance required) · Dental · 21 CFR 872.4920
## Classification
- **FDA Product Code:** EKZ
- **Device class:** Class II — Moderate Risk (510(k) clearance required)
- **Regulation:** 21 CFR 872.4920
- **Review panel:** DE
- **Medical specialty:** Dental
- **Submission type:** 1
- **GMP exempt:** N
- **Life sustaining:** N
- **Implant:** N
- **Third-party review:** Y
## Market data
- **Cleared 510(k) submissions:** 19
- **Registered establishments:** 9
## Source
- [FDA Device Classification](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpcd/classification.cfm?ID=EKZ)
---
*AI Analytics · CC0 1.0*