# NUELL, INC.

FEI: 1827813
Status: Active
Establishment types: Manufacture Medical Device for Another Party (Contract Manufacturer); Repack or Relabel Medical Device; Develop Specifications But Do Not Manufacture At This Facility; Manufacture Medical Device
Owner/operator: NUELL, INC. (#1827813)

Address: 312 EAST VAN BUREN ST., LEESBURG, IN, US



## Products

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

Proprietary names: DERMATOME BLADE

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%221827813%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=1827813