# REJONI, INC

FEI: 3033307563
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Manufacture Medical Device
Owner/operator: Rejoni, Inc (#10091756)

Address: 201 Burlington Rd, Bedford, MA, US



## Products

Total registered: 1
Top product codes: LKF
Regulation §: 884.4530

Proprietary names: Rejoni Acorn Catheter

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223033307563%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3033307563