# OSSTELL AB

FEI: 3004070020
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: OSSTELL AB (#9059818)

Address: Stampgaten 14, GOTEBORG Vastra Gotaland, 41101, SE

Mandatory US Agent: Pro Pharma Group

## Products

Total registered: 1
Top product codes: EKX
Regulation §: 872.4200

Proprietary names: Mega ISQ II, Beacon, Smart Pegs Type 1- 115, NeoTell, Osstell Classic, ISQTracker, SmartPeg Type 117, 127, 137

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223004070020%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3004070020