# PROSIDYAN, INC.

FEI: 3011015097
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Manufacture Medical Device
Owner/operator: Prosidyan, Inc. (#10047049)

Address: 41 Spring Street #107, New Providence, NJ, US



## Products

Total registered: 1
Top product codes: MQV
Regulation §: 888.3045

Proprietary names: FIBERGRAFT BG PUTTY

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223011015097%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3011015097