Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007031059

FEI Number

3007031059

Entity Name

ADEOR MEDICAL AG

City/State/Country

Valley Bavaria, DE

Establishment Address

Martinshof 5, Valley Bavaria D-83626, DE

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device

Owner / Operator

adeor medical AG (Owner Number: 10025686)

Owner / Operator Contact Address

adeor medical AG, Martinshof 5, Valley, DE-BY 83626, DE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K121253

PMA Number

N/A

All Registered Proprietary Names

adeor Zeppelin Microsurgical Instruments Velocity Alpha High Speed Drill System nxt bipolar forceps Atlas Choice bipolar forceps Velocity Alpha MR High Speed Surgical Drill System adeor Zeppelin Hysterectomy Clamps and Instruments adeor Meridian Cranial Perforator

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GZX	Instrument, Microsurgical	Neurology	Class 1	882.4525	2008-09-09
HBE	Drills, Burrs, Trephines & Accessories (Simple, Powered)	Neurology	Class 2	882.4310	2021-04-12
GEI	Electrosurgical, Cutting & Coagulation & Accessories	General, Plastic Surgery	Class 2	878.4400	2020-10-31
HBE	Drills, Burrs, Trephines & Accessories (Simple, Powered)	Neurology	Class 2	882.4310	2026-03-12
HBB	Motor, Drill, Pneumatic	Neurology	Class 2	882.4370	2026-03-12
KOH	Instrument, Manual, General Obstetric-Gynecologic	Obstetrics/Gynecology	Class 1	884.4520	2008-08-19
HBF	Drills, Burrs, Trephines & Accessories (Compound, Powered)	Neurology	Class 2	882.4305	2012-09-19

Official Correspondent

Fabio von Zeppelin

US Agent Details

Jim MacNee Business: USDeviceAgent.com Email: Jmacnee@USDeviceAgent.com Phone: (951) 8486626

Related Public Records

Same Entity

adeor medical AG

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
K970809	Somnus Medical Technologies, Inc.	BENDABLE TISSUE COAGULATING ELECTRODE WITH BENDING TOOL	1997-06-18
K222793	C.R. Bard, Inc.	WavelinQ Generator	2022-10-17
K002257	Tecno Instruments (Pvt.) , Ltd.	TECNO DISPOSABLE FINGERSWITCH PENCIL, MODEL 150-100	2000-10-19
K193591	Bowa-Electronics GmbH & Co. KG	ARC 400	2020-04-02
K192128	Sutter Medizintechnik GmbH	Sutter Arrowtip Monopolar Electrodes	2019-10-04

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0031-06	Rita Medical Systems	2	Rita Brand Habib 4X Electrosurgical Coagulator, Catalog Number: 4401US; Product is distributed by RITA Medical Systems, Inc., One Horizon Way. Manchester, GA 32826
Z-0026-2026	Aesculap AG Am Aesculap-Platz 1 Tuttlingen Germany	2	AESCULAP ELAN 4 FIXED DURAGUARD STANDARD. Model Number: GB942R.
Z-0027-2026	Aesculap AG Am Aesculap-Platz 1 Tuttlingen Germany	2	AESCULAP ELAN 4 FIXED DURAGUARD LONG. Model Number: GB943R.

Similar Registrations

Registration Number	Establishment Name	Location
3010707607	KARL STORZ SE & CO. KG	NEUHAUSEN OBECK Baden-Wurttemberg, DE
3036795921	KLS MARTIN SE & CO. KG	Fridingen Baden-Wurttemberg, DE
3000264417	Moria S.A	Bourbon l'Archambault Allier, FR
8010168	GEOMED MEDIZIN-TECHNIK GMBH & CO. KG	TUTTLINGEN Baden-Wurttemberg, DE
3002108226	SPIEGELBERG GmbH & Co. KG	Hamburg, DE

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007031059. Last updated year: 2026. Please use registration number 3007031059 when referencing this establishment in official correspondence.