# PLENOPTIKA EUROPE SLU

FEI: 3023983572
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: PLENOPTIKA EUROPE SLU (#10088304)

Address: Calle Faraday 7, Office 2.06, Madrid Madrid (Province), 28049, ES

Mandatory US Agent: PLENOPTIKA, INC.

## Products

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

Proprietary names: QuickSee Free Pro Keratometry, QuickSee Free

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223023983572%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3023983572