Biocomposites GmbH (former ARTOSS GmbH)

FDA Device Registration & Listing · Rostock Mecklenburg-Western Pomerania, DE · Registration 3011483489

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3011483489
FEI Number
3011483489
Entity Name
Biocomposites GmbH (former ARTOSS GmbH)
City/State/Country
Rostock Mecklenburg-Western Pomerania, DE
Establishment Address
Fischerweg 421, Rostock Mecklenburg-Western Pomerania 18069, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Biocomposites GmbH (former ARTOSS GmbH) (Owner Number: 10048987)
Owner / Operator Contact Address
Fischerweg 421, Rostock, DE-MV 18069, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

NanoBone SBX Putty NanoBone QD NanoBone SBX Putty NanoBone QD

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MQV Filler, Bone Void, Calcium Compound Orthopedic Class 2 888.3045 2019-06-06
MQV Filler, Bone Void, Calcium Compound Orthopedic Class 2 888.3045 2025-05-15

Official Correspondent

Imogen Carmichael

US Agent Details

Kathleen Moon Business: Biocomposites, Inc. Email: akm@biocomposites.com Phone: (910) 3508015

Related Public Records

Same Entity

Biocomposites GmbH (former ARTOSS GmbH)
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K180121 Cellumed Co., Ltd. Rafugen DBM 2018-04-11
K062691 Takiron Co., Ltd. COMPORUS 2008-04-15
K023703 Berkeley Advanced Biomaterials, Inc. BI-OSTETIC 2003-01-30
K173933 Xenco Medical, LLC Sorrento Bioglass Bone Graft Substitute 2018-09-13

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011483489. Last updated year: 2026. Please use registration number 3011483489 when referencing this establishment in official correspondence.
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