Product code LDG— Ear, Nose, Throat
COE-SIL
- Classification name
- Kit, Earmold, Impression
- Device class
- Class 1
- Regulation
- 21 CFR 874.3300
- Advisory panel
- Ear, Nose, Throat
- Total cleared
- 2
- First cleared
- Most recent
Market context for product code LDG
FDA has cleared devices under product code LDG between 1980 and 1983, filed by 2 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
- 1983
- 1980
Top applicants under product code LDG
Recent clearances under product code LDG
Data sourced from openFDA. This site is unofficial and independent of the FDA.