# MEBSTER Inc.

FEI: 3032847809
Status: Active
Establishment types: Repack or Relabel Medical Device; Manufacture Medical Device; Remanufacture Medical Device
Owner/operator: MEBSTER Inc. (#10091573)

Address: 101 W Dickman St, Baltimore, MD, US



## Products

Total registered: 1
Top product codes: IQI
Regulation §: 890.3475

Proprietary names: UNILEXA PRIME 2.1, UNILEXA HOME kit 2.1

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223032847809%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3032847809