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Medtec LLC

United States·US-MF-000002608

Last updated September 17, 2026

Information

Country: United States
Address: 1401, 8th Street SE, Orange City, United States
Website: cqmedical.com
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: +17127378688
PRRC Contact: Alena Newgren
EUDAMED SRN: US-MF-000002608
FDA FEI Number: 1000143606
DUNS Number: —

Catalogue (1098)

Page 13 of 22

Device	Model / Reference	Registries	Class	Status
Paddles	109012	FDA UDI	Class II	Unknown
Prone Shell	MT20215	FDA UDI	Class I	Unknown
IPPS™ Overlay	MTIL3013	FDA UDI	Class II	Active
MPC IsoCal Phantom Mount Assembly	MTIL6152	FDA UDI	Class II	Active
IPPS Overlay	MTIL6362	FDA UDI	Class II	Unknown
Vac-Lok™ Cushion	VL37	EUDAMEDFDA UDI	Class II	Active
Vac-Lok™ Cushion	VLA80C	EUDAMEDFDA UDI	Class II	Active
Knee-Lok Positioning Cushion	MTAKS02	FDA UDI	Class II	Unknown
Fiducial Markers	MTNW887854	FDA UDI	Class II	Unknown
Thermoplastic Frame	MTCFHN001	EUDAMEDFDA UDI	Class II	Active
Customizable Head Support	CHS01	EUDAMEDFDA UDI	Class II	Active
Vac-Lok™ Cushion	VLG35FC	EUDAMEDFDA UDI	Class II	Active
Uni-frame® Baseplate	MT20103CFU	EUDAMEDFDA UDI	Class II	Active
Positioning Cushion	301040	EUDAMEDFDA UDI	Class II	Active
Posicast® Thermoplastic	930080	EUDAMEDFDA UDI	Class II	Active
Vac-Lok Cushion	MTVLPLV01FC	FDA UDI	Class II	Unknown
Chabner XRT Radiation Bra	CRTBRA02	FDA UDI	Class II	Unknown
Posicast Thermoplastic	940044	FDA UDI	Class II	Unknown
Clamp	BPL006	FDA UDI	Class II	Unknown
Auto-Lok Assembly	MTSBRT032	FDA UDI	Class II	Unknown
Posifix® Headrest	301025BLK	EUDAMEDFDA UDI	Class II	Active
Prone Face Cushion	MTPFC01	FDA UDI	Class II	Unknown
IPPS™ Overlay	MTIL3301	FDA UDI	Class II	Unknown
Laser-Lok	MTSBRT037	FDA UDI	Class II	Unknown
Monarch™ Overhead Arm Positioner	OAP100	EUDAMEDFDA UDI	Class II	Active
Alloy Melter	MT803DEX	FDA UDI	Class I	Unknown
Vac-Lok™ Cushion	MTVLE2.25	FDA UDI	Class II	Unknown
Vac-Lok™ Cushion	MTVLWGB03	FDA UDI	Class II	Unknown
IPPS™ Couchtop	MTIL3601	FDA UDI	Class II	Active
Rails-only System	MTSBRT051	FDA UDI	Class II	Unknown
Body Pro-Lok ONE™ evo Adapter	BPL010	FDA UDI	Class II	Active
Template	MTM340520	FDA UDI	Class II	Unknown
Coupled™ Fiducial Marker Kit	MTNW887709	FDA UDI	Class II	Active
Headrest	MTTIMOF	FDA UDI	Class II	Unknown
Bolus	MTCB450S	FDA UDI	Class I	Unknown
Vac-Lok™ Cushion	VLG26C	EUDAMEDFDA UDI	Class II	Active
Clam-Lok Cushion	MTSBRT202	FDA UDI	Class II	Unknown
IPPS™ Couchtop	MTIL3603	FDA UDI	Class II	Unknown
Vac-Lok™ Vacuum Compressor	MTVPHD	FDA UDI	Class II	Unknown
Vac-Lok™ Vacuum Compressor	MTVP1	EUDAMEDFDA UDI	Class II	Active
Vac-Lok™ Vacuum Compressor	MTVPHS	FDA UDI	Class II	Active
Body Bridge	MTM300110	FDA UDI	Class II	Active
Vac-Lok™ Cushion	VLG40C	EUDAMEDFDA UDI	Class II	Active
Fiducial Marker Kit	MTNW887830	EUDAMEDFDA UDI	Class II	Active
Posifix® -5 Baseplate	105021	FDA UDI	Class II	Active
Vac-Lok™ Cushion	VLPLV02C	EUDAMEDFDA UDI	Class II	Active
Posifix® Headrest	301025	FDA UDI	Class II	Unknown
ProForm™ Head and Neck Extension	MTIL6675	FDA UDI	Class II	Active
IPPS Overlay	MTIL6063	FDA UDI	Class II	Unknown
Protura	MT6XSM1.5.0	FDA UDI	Class II	Unknown

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FDA Recalls (14)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Date	Recall No.	Class	Status	Reason
May 12, 2020	Z-2243-2020	—	terminated	Potential for disengagement of the Varian Style Type-S Extension during patient repositioning. The risk associated with the disengagement of the extension could be a patient fall if the patient is not supported by clinical staff.
Apr 15, 2019	Z-1837-2019	—	terminated	There is a potential for movement of the Solstice Tilting Head Fixation System during patient setup and/or treatment.
Nov 8, 2017	Z-0671-2018	—	terminated	When an error message remains displayed and is not cleared in the Protura software with the Elekta pedestal coordinates, moving the pedestal could cause the Protura software to not update with the pedestal location and buffers the pedestal movement history.
Aug 10, 2017	Z-3082-2017	—	terminated	Rigid Arm Supports (PN: 106015 and 106047), which were used as part of the Posiboard-2 and Posirest, and were distributed as PN: 106015, 106047, 106521, 106522, 109030, and 109040 between Ocotober 2009 and July 2012 may have a height difference of approximately 17mm.
Aug 10, 2017	Z-3083-2017	—	terminated	Rigid Arm Supports (PN: 106015 and 106047), which were used as part of the Posiboard-2 and Posirest, and were distributed as PN: 106015, 106047, 106521, 106522, 109030, and 109040 between Ocotober 2009 and July 2012 may have a height difference of approximately 17mm.
Mar 31, 2016	Z-1992-2016	—	terminated	When using the recalled product in split shift mode, the non-sub-millimeter positioning has been found to be inconsistent with the setting parameters.
Aug 19, 2015	Z-2763-2015	—	terminated	The wrist straps used for positioning the patient are too long
Dec 11, 2014	Z-0989-2015	—	terminated	The product (wool wrist loop) was manufactured 7cm shorter than product specifications.
Dec 11, 2014	Z-0990-2015	—	terminated	The product (wool wrist loop) was manufactured 7cm shorter than product specifications.
Jun 21, 2010	Z-0394-2011	—	terminated	Under certain conditions, the extensions can become detached from the main body of the couch.
Jun 21, 2010	Z-0395-2011	—	terminated	Under certain conditions, the extensions can become detached from the main body of the couch.
Jun 21, 2010	Z-0396-2011	—	terminated	Under certain conditions, the extensions can become detached from the main body of the couch.
Aug 31, 2009	Z-0124-2010	—	terminated	Some of the packages contain the incorrect mask style.
Mar 6, 2009	Z-1721-2009	—	terminated	The silkscreened indexing scale was reversed.