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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 10 of 22

Device	Model / Reference	Registries	Class	Status
IPPS Overlay	20IL430135	FDA UDI	Class II	Unknown
Body Pro-Lok ONE™ System	BPL110	FDA UDI	Class II	Unknown
AccuForm™ Cushion	MTACL2035HF	FDA UDI	Class II	Active
Vac-Lok™ Cushion	VLWGB05C	EUDAMEDFDA UDI	Class II	Active
Prodigy™ Lok-Bar™	MTIL3653	FDA UDI	Class II	Active
Universal Couchtop	MTIL6064	FDA UDI	Class II	Unknown
IPPS™ Overlay	MTM3405	FDA UDI	Class II	Active
Fiducial Marker Kit	MTNW887871	EUDAMEDFDA UDI	Class II	Active
IPPS™ Overlay	MTM3301	FDA UDI	Class II	Unknown
Prodigy™ 2 Lok-Bar™	MTIL6051	FDA UDI	Class II	Active
Docking Station	MTIL301310	FDA UDI	Class II	Unknown
Clamp	MTSBRT256	EUDAMEDFDA UDI	Class II	Active
IPPS™ Overlay	MTM330110	FDA UDI	Class II	Unknown
Vac-Lok™ Cushion	VLPLV10FC	EUDAMEDFDA UDI	Class II	Active
Posicast® Thermoplastic	976150	FDA UDI	Class II	Unknown
Headrest - TIMO Size A, B, C, D, E, F	MTTIMO2	EUDAMEDFDA UDI	Class II	Active
Uni-frame® Thermoplastic	MTAPU12	EUDAMEDFDA UDI	Class II	Active
Lok-Bar™	MTSBRT055	FDA UDI	Class II	Active
Posicast® Thermoplastic	930033	EUDAMEDFDA UDI	Class II	Active
Fiducial Markers	MTNW887809	FDA UDI	Class II	Active
Protura	206X140	FDA UDI	Class II	Unknown
trUpoint ARCH Replacement Kit	MTHF175	FDA UDI	Class II	Unknown
Body Pro-Lok™ Platform	MTSBRT002	EUDAMEDFDA UDI	Class II	Active
Prodigy™ 2 Lok-Bar™	MTIL6056	FDA UDI	Class II	Active
Respiratory Plate	BPL008	EUDAMEDFDA UDI	Class II	Active
Positioning Cushion	301076	FDA UDI	Class II	Active
Spacer	107104MR	EUDAMEDFDA UDI	Class II	Active
Body Pro-Lok™ Bridge	MTSBRT031	FDA UDI	Class II	Active
Type-S™ Thermoplastic	MTAPSP2.4	EUDAMEDFDA UDI	Class II	Active
Posiboard™	109030	FDA UDI	Class II	Unknown
Couchtop Panel	MTIL3103	FDA UDI	Class II	Unknown
Headrest - Timo size B	MTTIMO2B	EUDAMEDFDA UDI	Class II	Active
ProForm™ CT Overlay	PRO310	FDA UDI	Class II	Unknown
IPPS Overlay	MTIL6363	FDA UDI	Class II	Unknown
Docking Station	MTIL630110	FDA UDI	Class II	Unknown
IPPS™ Overlay	MTM3400	FDA UDI	Class II	Unknown
Uni-frame® Baseplate	MT20100CF	EUDAMEDFDA UDI	Class II	Active
Uni-frame® Thermoplastic	MTAPUIW1832VT	EUDAMEDFDA UDI	Class II	Active
Vac-Lok™ Cushion	VLARM02	FDA UDI	Class II	Unknown
Vac-Lok Cushion	MTVLWGB03C	FDA UDI	Class II	Unknown
Butt Stop Bar Replacement Set	MT350N027	FDA UDI	Class II	Unknown
TotalRT All In One Platform	TRT100	FDA UDI	Class II	Active
Fiducial Marker Kit	MTNW887866	FDA UDI	Class II	Active
Vac-Lok™ Cushion	MTVLPLV01	FDA UDI	Class II	Unknown
Posicast® Thermoplastic	930044	EUDAMEDFDA UDI	Class II	Active
Immobilizer	MTDLIZ	FDA UDI	Class II	Unknown
Positioning Cushion	301081	EUDAMEDFDA UDI	Class II	Active
IPPS Overlay	MTIL4300	FDA UDI	Class II	Unknown
Couchtop Panel	MTIL301001	FDA UDI	Class II	Unknown
McLaurin Arch	MTPT1002	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.