# LGM INTERNATIONAL INC.

FEI: 3004421347
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: LGM INTERNATIONAL INC. (#9059951)

Address: 295 North Dr Ste A, Melbourne, FL, US



## Products

Total registered: 1
Top product codes: PPM
Regulation §: 864.4010

Proprietary names: LIQUI-PREP SPECIAL PROCESSING KIT, LIQUI-PREP CYTOLOGY PROCESSING SYST

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223004421347%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3004421347