Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1643116

FEI Number

1643116

Entity Name

voss medical products

City/State/Country

San Antonio, TX, US

Establishment Address

4235 centergate, San Antonio, TX 78217, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

VOSS MEDICAL PRODUCTS (Owner Number: 1643116)

Owner / Operator Contact Address

4235 CENTERGATE, --, San Antonio, TX 78217, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K932187

PMA Number

N/A

All Registered Proprietary Names

Coronary Bypass Graft Marker 7" Round Support Voss Supine Head Positioner Voss Laminectomy Arm Cradle Clamp, Vascular Wulfsohn Disposable Laryngoscope The Voss Cervical Laminectomy Harness The Voss CLH CLH Voss Chest Roll Coronary Bypass Flushing Cannula Cervical Laminectomy Harness Voss Bypass Leg Positioner Voss Cardiac Leg Support Voss Convoluted Arm Board Voss 9" Round Support Voss Small Bolster PronePositioner

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KPK	Marker, Ostia, Aorto-Saphenous Vein	General, Plastic Surgery	Class 2	878.4650	2007-12-07
PRN	Pediatric Position Holder	General Hospital	Class 1	880.5680	2018-05-17
CCX	Support, Patient Position	Anesthesiology	Class 1	868.6820	2018-05-17
BTX	Board, Arm (With Cover), Sterile	General, Plastic Surgery	Class 1	878.3910	2018-05-17
DXC	Clamp, Vascular	Cardiovascular	Class 2	870.4450	2007-12-07
CCW	Laryngoscope, Rigid	Anesthesiology	Class 1	868.5540	2013-08-13
IQF	Orthosis, Cervical-Thoracic, Rigid	Physical Medicine	Class 1	890.3490	2014-09-19
NXH	Nursing Pad, Cohesive Gel	General Hospital	Class 1	880.5630	2018-05-17
DWF	Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass	Cardiovascular	Class 2	870.4210	2007-12-07
IQK	Orthosis, Cervical	Physical Medicine	Class 1	890.3490	2013-08-28
FQO	Table, Operating-Room, Ac-Powered	General, Plastic Surgery	Class 1	878.4960	2011-12-22
NOD	Board, Arm (With Cover), Non-Sterile	General, Plastic Surgery	Class 1	878.3910	2018-05-17
EPW	Support, Head, Surgical, Ent	General, Plastic Surgery	Class 1	878.4950	2018-05-17
FQL	Stocking, Medical Support (For General Medical Purposes)	General Hospital	Class 1	880.5780	2018-05-17
KIL	Positioner, Socket	Orthopedic	Class 1	888.4540	2011-12-22

Official Correspondent

SARA VOSS

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

VOSS MEDICAL PRODUCTS

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
K832124	Med-West, Inc.	CPC, COUBLE LUMEN CARDIOPLEGIA-AIR ASPI	1983-08-12
K162500	Spyder Medical	Ostial Sprit Cannulae	2017-01-12

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0144-2024	Covidien	1	Stolen McGRATH MAC Video Laryngoscopes, REF: 301-000-000
Z-0168-2024	Covidien	1	McGrath Mac 2, Disposable Laryngoscope Blade, REF: 350-017-000, Sterile EO, Rx Only
Z-0169-2024	Covidien	1	McGrath Mac 2, Disposable Laryngoscope Blade, REF: 350-084-000, Sterile EO, Rx Only
Z-0003-2022	Medtronic Perfusion Systems	2	Medtronic Bio-Medicus Insertion Kits, Model number 96553, Pediatric Insertion Kit, Sterile; and Model number 96551, Venous Insertion Kit, Sterile.
Z-0021-2018	OriGen Biomedical, Inc.	2	The OriGen Reinforced Dual Lumen catheter (RDLC) is a duel lumen catheter with a wire reinforcement layer on the tip of the device. A thin sheath is used to cover and secure the wire layer and is heat shrunk into a permanent position.

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3003102481	MARKETLAB INCORPORATED	Caledonia, MI, US
3016750643	MEGAFORCE COMPANY LIMITED	New Taipei City, TW
3014680784	Domico Med-Device, LLC	Fenton, MI, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1643116. Last updated year: 2026. Please use registration number 1643116 when referencing this establishment in official correspondence.