# PLUSOPTIX GMBH

FEI: 3003829667
Status: Active
Establishment types: Develop Specifications But Do Not Manufacture At This Facility; Manufacture Medical Device
Owner/operator: PLUSOPTIX GMBH (#9050572)

Address: Nordostpark 21, Nuremberg Bavaria, 90411, DE

Mandatory US Agent: Plusoptix Inc.

## Products

Total registered: 1
Top product codes: HKO
Regulation §: 886.1760

Proprietary names: plusoptiX S20, plusoptiX A12, PowerRef 3, plusoptiX PR3, plusoptiX S16, plusoptiX A16, plusoptiX S12, plusoptiX A20

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223003829667%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3003829667