# KREYENBERG GMBH

FEI: 3009455196
Status: Active
Establishment types: Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner/operator: Kreyenberg GmbH (#10044509)

Address: Oststrasse 51, Norderstedt Schleswig-Holstein, D-22844, DE

Mandatory US Agent: Emergo Global Consulting LLC

## Products

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

Proprietary names: SPEEDLOCK SLEEVE 200, SPEEDLOCK SLEEVE 180, SPEEDLOCK SLEEVE 170, Artemis - Lag screw guide sleeve, Artemis - Repositioning guide sleeve, Artemis - Channel tube

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223009455196%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3009455196