CURASAN AG

FDA Device Registration & Listing · KLEINOSTHEIM Bavaria, DE · Registration 3003771570

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
3003771570
FEI Number
3003771570
Entity Name
CURASAN AG
City/State/Country
KLEINOSTHEIM Bavaria, DE
Establishment Address
LINDIGSTRASSE 4, KLEINOSTHEIM Bavaria 63801, DE
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
curasan AG (Owner Number: 10034158)
Owner / Operator Contact Address
Lindigstrasse 4, Kleinostheim, DE-BY 63801, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

IngeniOs HA Osbone Dental Cerasorb Dental Osseolive DENTAL Ceracell Ortho Foam Matriform Si Strip VerteFrame TriForm Cerasorb Ortho Foam Matriform

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LYC Bone Grafting Material, Synthetic Dental Class 2 872.3930 2011-03-10
LYC Bone Grafting Material, Synthetic Dental Class 2 872.3930 2010-11-11
LYC Bone Grafting Material, Synthetic Dental Class 2 872.3930 2013-11-27
MQV Filler, Bone Void, Calcium Compound Orthopedic Class 2 888.3045 2018-12-20
MQV Filler, Bone Void, Calcium Compound Orthopedic Class 2 888.3045 2016-12-15

Official Correspondent

Steffi Manig

US Agent Details

Daryl Wisdahl Business: MedEnvoy Global Inc. Email: usagent@medenvoyglobal.com Phone: (512) 2560570

Related Public Records

Same Entity

curasan AG
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3004847139 CURASAN AG, FRANKFURT FACILITY FRANKFURT Hesse, DE

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K052493 Steiner Laboratories SOCKET GRAFT 2006-06-09
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 3003771570. Last updated year: 2026. Please use registration number 3003771570 when referencing this establishment in official correspondence.
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