# POSITRIGO AG

FEI: 3032577207
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Export Device to the United States But Perform No Other Operation on Device; Develop Specifications But Do Not Manufacture At This Facility; Manufacture Medical Device
Owner/operator: Positrigo AG (#10091382)

Address: Technoparkstrasse 1, Zurich, 8005, CH

Mandatory US Agent: Positrigo Inc.

## Products

Total registered: 1
Top product codes: KPS
Regulation §: 892.1200

Proprietary names: NeuroLF Seat, NeuroLF (Basic), NeuroLF (Pro), NeuroLF (Advanced)

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223032577207%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3032577207