# Acuity Pro, Inc.

FEI: 3014267863
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Manufacture Medical Device
Owner/operator: Acuity Pro, Inc. (#10056694)

Address: 920 N Main St, Elk City, OK, US



## Products

Total registered: 1
Top product codes: HOX
Regulation §: 886.1150

Proprietary names: Acuity Pro

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223014267863%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3014267863