# LUTHER NEEDLESAFE PRODUCTS LLC

FEI: 3017129766
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: Luther Needlesafe Products LLC (#10087391)

Address: 26052 Merit Cir Ste 107, Laguna Hills, CA, US



## Products

Total registered: 1
Top product codes: FOZ
Regulation §: 880.5200

Proprietary names: Mini-Midline Extended Dwell Peripheral Catheter

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223017129766%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3017129766