# INCREMED AG

FEI: 3020521079
Status: Active
Establishment types: Develop Specifications But Do Not Manufacture At This Facility; Manufacture Medical Device
Owner/operator: Incremed AG (#10082674)

Address: Bubenbergstrasse 1, Zurich, 8045, CH

Mandatory US Agent: Regulatory Insight, Inc.

## Products

Total registered: 1
Top product codes: LMD
Regulation §: 892.2020

Proprietary names: OptiVu Streamer R2.1, SonoEyes R2, OptiVu Streamer R2

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223020521079%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3020521079