FDA Device Establishments · JSON-LD · Markdown

KREYENBERG GMBH

FEI 3009455196 · Manufacture Medical Device for Another Party (Contract Manufacturer) · Status: Active

FEI Number3009455196
Owner / OperatorKreyenberg GmbH (#10044509)
AddressOststrasse 51, Norderstedt Schleswig-Holstein, D-22844, DE
Mandatory US AgentEmergo Global Consulting LLC
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)LXH
Regulation § (21 CFR)888.4540
Proprietary namesSPEEDLOCK SLEEVE 200; SPEEDLOCK SLEEVE 180; SPEEDLOCK SLEEVE 170; Artemis - Lag screw guide sleeve; Artemis - Repositioning guide sleeve; Artemis - Channel tube

External sources

Source: openFDA. Public-domain (CC0).