# Medynus, Inc.

FEI: 3015426608
Status: Active
Establishment types: Manufacture Medical Device; Develop Specifications But Do Not Manufacture At This Facility; Complaint File Establishment per 21 CFR 820.198
Owner/operator: Medynus, Inc. (#10060045)

Address: 18 Technology Dr. Suite 109, Irvine, CA, US



## Products

Total registered: 2
Top product codes: ODP, MAX
Regulation §: 888.3080

Proprietary names: CCN-00013 (AC.2109) ACDF Trial (Lordotic) L14 x W14 x A7 x H9, CCN-00011 (AC.2107) ACDF Trial (Lordotic) L14 x W14 x A7 x H7, Pixie (ACIF, DLIF, PLIF, TLIF, ALIF) PEEK Cage, Cervical Cage Container (CCT-00001), Trial Anatomic dual 14*16*11-12mm, Trial Lordotic dual 14*16*5-6mm, Trial Lordotic dual 12*14*11-12mm, Trial Anatomic 14*16*10mm (CCN-00030), Trial Lordotic 12*14*8mm (CCN-00004), Trial Anatomic 14*16*9mm (CCN-00029)

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223015426608%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3015426608