# PRO-DEX, INC.

FEI: 2081135
Status: Active
Establishment types: Manufacture Medical Device for Another Party (Contract Manufacturer); Complaint File Establishment per 21 CFR 820.198; Manufacture Medical Device
Owner/operator: PRO-DEX, INC. (#2081135)

Address: 2361 McGaw Avenue, Irvine, CA, US



## Products

Total registered: 1
Top product codes: GEY
Regulation §: 878.4820

Proprietary names: Pro-Dex Surgical Driver (PDSD-5000-X), PDCMF Power Driver (PDCMF-1000-X), Atlas Pro Driver Hex Collet (APD-CA-001-1), Atlas Pro Driver (APD-1000-1), Atlas Pro Driver Battery Single Use Battery Case (APD-BP-010S-1), Pro-Dex Surgical Driver, Single Pouch Battery Pack (PDBP-001-X; PDBP-010-X; PDBD-040-X)

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%222081135%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=2081135