# BIOPTRON AG

FEI: 3013929417
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: BIOPTRON AG (#9052406)

Address: Gouttes d Or 30, Neuchatel, 2008, CH

Mandatory US Agent: REGULATORY INSIGHT, INC.

## Products

Total registered: 1
Top product codes: NHN
Regulation §: 890.5500

Proprietary names: BIOPTRON MedAll, BIOPTRON PRO 1 (BPro1) Light Therapy System, BIOPTRON Pro (BPro) Light Therapy System, BIOPTRON 2 (B2) Light Therapy System, BIOPTRON Compact III (BCIII) Light Therapy System

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223013929417%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3013929417