# ActiGraph L.L.C.

FEI: 3006254866
Status: Active
Establishment types: Repack or Relabel Medical Device; Develop Specifications But Do Not Manufacture At This Facility; Manufacture Medical Device
Owner/operator: ActiGraph, LLC (#10023162)

Address: 70 North Baylen Street, Suite 400, Pensacola, FL, US



## Products

Total registered: 5
Top product codes: DQA, MWI, MSX, DRG, BZQ
Regulation §: 870.2700, 870.2300, 870.2910, 868.2375

Proprietary names: Everion+ (G2) System

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223006254866%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3006254866