# OSTEOTEC LIMITED

FEI: 3008395366
Status: Active
Establishment types: Export Device to the United States But Perform No Other Operation on Device; Develop Specifications But Do Not Manufacture At This Facility
Owner/operator: Osteotec Limited (#10032513)

Address: Building 81, Greenham Business Park, Newbury West Berkshire, RG19 6HW, GB

Mandatory US Agent: TriMed Inc

## Products

Total registered: 1
Top product codes: HTQ
Regulation §: 888.4540

Proprietary names: Osteotec Silicone Finger Rasp

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223008395366%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3008395366