# POWDER DESIGN, LTD

FEI: 3015905920
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Repack or Relabel Medical Device; Export Device to the United States But Perform No Other Operation on Device
Owner/operator: Powder Design, LTD (#10084120)

Address: 17/1 Silvermills Court, Henderson Place Lane, Edinburgh Midlothian, EH3 5DG, GB

Mandatory US Agent: Registrar Corp

## Products

Total registered: 1
Top product codes: HQY
Regulation §: 886.5850

Proprietary names: Powder

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223015905920%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3015905920