mebios GmbH

FDA Device Registration & Listing · Dieburg Hesse, DE · Registration 3015131160

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
3015131160
FEI Number
3015131160
Entity Name
mebios GmbH
City/State/Country
Dieburg Hesse, DE
Establishment Address
Lagerstr. 11, Haus C, Dieburg Hesse 64807, DE
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
botiss biomaterials GmbH (Owner Number: 10058419)
Owner / Operator Contact Address
Hauptstrasse 28, Zossen, DE-BB 15806, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Straumann cerabone cerabone

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NPM Bone Grafting Material, Animal Source Dental Class 2 872.3930 2018-12-18

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar corp Email: David.Lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

botiss biomaterials GmbH
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3014206569 BOTISS BIOMATERIALS GMBH Zossen Brandenburg, DE

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015131160. Last updated year: 2026. Please use registration number 3015131160 when referencing this establishment in official correspondence.
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