Data / Medical devices / Germany / VBM Medizintechnik GMBH

VBM Medizintechnik GMBH: FDA-registered device maker in SULZ AM NECKAR Baden-Wurttemberg, Germany, 4 510(k) clearances

Name: VBM Medizintechnik GMBH FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

VBM Medizintechnik GMBH is registered with the FDA (registration 8010939) in SULZ AM NECKAR Baden-Wurttemberg, Germany. It lists 23 device types. The FDA files 4 510(k) clearances under its listings, the newest dated October 30, 2020. Registered through 2027. FDA data exported November 2, 2026.

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FDA registration number: 8010939
FEI number: 3002808440
Address: 1, Einsteinstrasse, SULZ AM NECKAR Baden-Wurttemberg, Germany, 72172
Owner or operator: VBM Medizintechnik GmbH (8010939)
Roles: Contract manufacturer, Manufacturer
First device listed: March 28, 1997
Registered through: 2027
Brand names listed: 00-197, 01-00-100, 01-00-110, 01-15-000, 01-20-000, 03-42-902, 03-43-902, 10-12-800-VK and more

Devices it lists

Device	Product code	Class	Role	Source
Airway, Oropharyngeal, Anesthesiology	CAE	1	Contract manufacturer, Manufacturer	accessdata.fda.gov
Apparatus, Suction, Single Patient Use, Portable, Nonpowered	GCY	1	Manufacturer	accessdata.fda.gov
Bag, Reservoir	BTC	1	Manufacturer	accessdata.fda.gov
Bandage, Elastic	FQM	1	Manufacturer	accessdata.fda.gov
Circuit, Breathing (W Connector, Adaptor, Y Piece)	CAI	1	Manufacturer	accessdata.fda.gov
Connector, Airway (Extension)	BZA	1	Contract manufacturer, Manufacturer	accessdata.fda.gov
Cuff, Tracheal Tube, Inflatable	BSK	2	Manufacturer	accessdata.fda.gov
Device, Fixation, Tracheal Tube	CBH	1	Manufacturer	accessdata.fda.gov
Device, Rebreathing	BYW	1	Manufacturer	accessdata.fda.gov
Humidifier, Respiratory Gas, (Direct Patient Interface)	BTT	2	Contract manufacturer	accessdata.fda.gov
Infusor, Pressure, For I.V. Bags	KZD	1	Manufacturer	accessdata.fda.gov
Laryngoscope, Rigid	CCW	1	Contract manufacturer	accessdata.fda.gov
Mask, Gas, Anesthetic	BSJ	1	Manufacturer	accessdata.fda.gov
Needle, Emergency Airway	BWC	2	Manufacturer	accessdata.fda.gov
Orthosis, Sacroiliac, Soft	IPW	1	Manufacturer	accessdata.fda.gov
Set, Tubing And Support, Ventilator (W Harness)	BZO	1	Manufacturer	accessdata.fda.gov
Strap, Head, Gas Mask	BTK	1	Manufacturer	accessdata.fda.gov
Stylet, Tracheal Tube	BSR	1	Manufacturer	accessdata.fda.gov
Support, Breathing Tube	JAY	1	Manufacturer	accessdata.fda.gov
Tourniquet, Pneumatic	KCY	1	Manufacturer	accessdata.fda.gov
Tube Tracheostomy And Tube Cuff	JOH	2	Manufacturer	accessdata.fda.gov
Tube, Tracheostomy (W/Wo Connector)	BTO	2	Manufacturer	accessdata.fda.gov
Ventilator, Continuous, Facility Use	CBK	2	Contract manufacturer	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
October 30, 2020	K200190	ScalpelCric	BWC	Substantially Equivalent	VBM Medizintechnik GmbH	accessdata.fda.gov
March 19, 1997	K955461	TRANSTRACHEAL CATHETER (ACC. RAVUSSIN).	BTO	Substantially Equivalent	VBM Medizintechnik GmbH	accessdata.fda.gov
July 20, 1991	K912723	POSEY CUFFLATOR	BSK	Substantially Equivalent	Posey Co.	accessdata.fda.gov
December 31, 1987	K874742	QUICKTRACH	BTO	Substantially Equivalent	Posey Co.	accessdata.fda.gov

Compare with other makers

Updated October 30, 2020. 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.