Data / Medical devices / United States / voss medical products

voss medical products: FDA-registered device maker in San Antonio, TX, United States, 5 510(k) clearances

Name: voss medical products FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

voss medical products is registered with the FDA (registration 1643116) in San Antonio, TX, United States. It lists 17 device types. The FDA files 5 510(k) clearances under its listings, the newest dated June 1, 1993. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 1643116
Address: 4235 centergate, San Antonio, TX, United States, 78217
Owner or operator: VOSS MEDICAL PRODUCTS (1643116)
Roles: Manufacturer, Specification developer
First device listed: December 7, 2007
Registered through: 2026
Brand names listed: 7" Round Support, CLH, Cervical Laminectomy Harness, Clamp, Vascular, Coronary Bypass Flushing Cannula, Coronary Bypass Graft Marker, PronePositioner, The Voss CLH and more

Devices it lists

Device	Product code	Class	Role	Source
Board, Arm (With Cover), Non-Sterile	NOD	1	Specification developer	accessdata.fda.gov
Board, Arm (With Cover), Sterile	BTX	1	Specification developer	accessdata.fda.gov
Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass	DWF	2	Manufacturer	accessdata.fda.gov
Clamp, Vascular	DXC	2	Manufacturer	accessdata.fda.gov
Headrest, Neurosurgical	HBM	1	Specification developer	accessdata.fda.gov
Kit, Surgical Instrument, Disposable	KDD	1	Specification developer	accessdata.fda.gov
Laryngoscope, Rigid	CCW	1	Specification developer	accessdata.fda.gov
Marker, Ostia, Aorto-Saphenous Vein	KPK	2	Manufacturer	accessdata.fda.gov
Nursing Pad, Cohesive Gel	NXH	1	Specification developer	accessdata.fda.gov
Orthosis, Cervical	IQK	1	Manufacturer	accessdata.fda.gov
Orthosis, Cervical-Thoracic, Rigid	IQF	1	Manufacturer	accessdata.fda.gov
Pediatric Position Holder	PRN	1	Specification developer	accessdata.fda.gov
Positioner, Socket	KIL	1	Manufacturer	accessdata.fda.gov
Stocking, Medical Support (For General Medical Purposes)	FQL	1	Specification developer	accessdata.fda.gov
Support, Head, Surgical, Ent	EPW	1	Specification developer	accessdata.fda.gov
Support, Patient Position	CCX	1	Specification developer	accessdata.fda.gov
Table, Operating-Room, Ac-Powered	FQO	1	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
June 1, 1993	K932187	PRONE POSITIONER	KIL	Substantially Equivalent	Voss Medical Products	accessdata.fda.gov
June 1, 1993	K932186	BYPASS LEG POSITIONER	FQO	Substantially Equivalent	Voss Medical Products	accessdata.fda.gov
May 17, 1990	K896338	VOSS DISPOSABLE CORONARY BYPASS FLUSHING CANNULA	DWF	Substantially Equivalent	Voss Medical Products	accessdata.fda.gov
December 22, 1989	K885161	VOSS VEIN CLAMP	DXC	Substantially Equivalent	Voss Medical Products	accessdata.fda.gov
September 27, 1989	K895369	VOSS GRAFT MARKER	KPK	Substantially Equivalent	Voss Medical Products	accessdata.fda.gov

Compare with other makers

Updated June 1, 1993. 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.