Data / Medical devices / Germany / Adeor Medical AG

Adeor Medical AG: FDA-registered device maker in Valley Bavaria, Germany, 5 510(k) clearances

Name: Adeor Medical AG FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Adeor Medical AG is registered with the FDA (registration 3007031059) in Valley Bavaria, Germany. It lists 6 device types. The FDA files 5 510(k) clearances under its listings, the newest dated March 6, 2026. Registered through 2027. FDA data exported November 2, 2026.

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FDA registration number: 3007031059
Address: Martinshof 5, Valley Bavaria, Germany, D-83626
Owner or operator: adeor medical AG (10025686)
Roles: Complaint file establishment, Manufacturer, Specification developer
First device listed: August 19, 2008
Registered through: 2027
Brand names listed: Atlas Choice bipolar forceps, HiCUT Highspeed Cutters, Velocity Alpha High Speed Drill System, Velocity Alpha MR High Speed Surgical Drill System, adeor Meridian Cranial Perforator, adeor Zeppelin Hysterectomy Clamps and Instruments, adeor Zeppelin Microsurgical Instruments, nxt bipolar forceps

Devices it lists

Device	Product code	Class	Role	Source
Drills, Burrs, Trephines & Accessories (Compound, Powered)	HBF	2	Complaint file establishment, Manufacturer	accessdata.fda.gov
Drills, Burrs, Trephines & Accessories (Simple, Powered)	HBE	2	Complaint file establishment, Specification developer	accessdata.fda.gov
Electrosurgical, Cutting & Coagulation & Accessories	GEI	2	Complaint file establishment, Specification developer	accessdata.fda.gov
Instrument, Manual, General Obstetric-Gynecologic	KOH	1	Complaint file establishment, Specification developer	accessdata.fda.gov
Instrument, Microsurgical	GZX	1	Complaint file establishment, Specification developer	accessdata.fda.gov
Motor, Drill, Pneumatic	HBB	2	Complaint file establishment, Specification developer	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
March 6, 2026	K253772	Velocity Alpha MR High Speed Surgical Drill System	HBB	Substantially Equivalent	Adeor Medical AG	accessdata.fda.gov
April 11, 2021	K191479	Velocity Alpha Highspeed Surgical Drill System	HBE	Substantially Equivalent	Adeor Medical AG	accessdata.fda.gov
May 22, 2020	K191847	Adeor Medical nxt Non-stick Bipolar Forceps, Adeor Medical nxt Single-Use Non-stick Bipolar Forceps	GEI	Substantially Equivalent	Adeor Medical AG	accessdata.fda.gov
June 27, 2014	K130755	HICUT HIGHSPEED INSTRUMENT	HBE	Substantially Equivalent	Adeor Medical AG	accessdata.fda.gov
July 17, 2012	K121253	MERIDIAN CRANIAL PERFORATOR	HBF	Substantially Equivalent	Adeor Medical Technologies GmbH	accessdata.fda.gov

Compare with other makers

Updated March 6, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.