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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 7 of 22

Device	Model / Reference	Registries	Class	Status
Lateral Stabilizer	MTIL630211	FDA UDI	Class II	Active
Vac-Lok Cushion	MTVLARM01C	FDA UDI	Class II	Unknown
Protura 1.7.1	MT6XSM1.7.1	FDA UDI	Class II	Unknown
Cushion Guide	PRO350	EUDAMEDFDA UDI	Class II	Active
Prodigy Lok-Bar	20IL430020	FDA UDI	Class II	Unknown
Headrest	MTTIMOEL	FDA UDI	Class II	Unknown
Locators	109038	FDA UDI	Class II	Unknown
Adjustable Backrest	MTIL7115	FDA UDI	Class II	Active
Pro Wing Board™	OAP220	FDA UDI	Class II	Active
Docking Station	MTIL600210	FDA UDI	Class II	Active
Hip Stop	MT350300	EUDAMEDFDA UDI	Class II	Active
Locators	109027	FDA UDI	Class II	Unknown
Headrest - Timo size A with base	MTTIMO2AL	EUDAMEDFDA UDI	Class II	Active
Arm Support	MTTAS2R	EUDAMEDFDA UDI	Class II	Active
ProForm™ Thermoplastic	PRO330SPN32	EUDAMEDFDA UDI	Class II	Active
Proutra™	MT6XCALS	FDA UDI	Class II	Active
Vac-Lok Hook	MTVLHOOK	FDA UDI	Class II	Unknown
Solstice™ MR SRS Immobilization System	CHS04MR	EUDAMEDFDA UDI	Class II	Active
Pro Handle	OAP221	EUDAMEDFDA UDI	Class II	Active
ProForm™ Thermoplastic	PRO331IM1832N	EUDAMEDFDA UDI	Class II	Active
Body Pro-Lok ONE™ Rails-Only System	BPL020	EUDAMEDFDA UDI	Class II	Active
Headrest - TIMO Size A, B, C, F	MTTIMO2L	EUDAMEDFDA UDI	Class II	Active
AccuForm™ Cushion	MTACLTYPESN	FDA UDI	Class II	Unknown
Patient Hand Grip	MTIL662501	FDA UDI	Class II	Active
Posicast® Thermoplastic	770145	FDA UDI	Class II	Unknown
Type-S™ Thermoplastic	MTAPSID2924	EUDAMEDFDA UDI	Class II	Active
Bolus	MTCB305005S	FDA UDI	Class I	Unknown
Vac-Lok™ Cushion	MTVLFBB01	FDA UDI	Class II	Unknown
Assist Handles	622510	FDA UDI	Class II	Unknown
Posiboard™	109020	FDA UDI	Class II	Unknown
Head Bridge	MTM300205	FDA UDI	Class II	Active
Uni-frame® Thermoplastic	MTAPUR	EUDAMEDFDA UDI	Class II	Active
Locators	662030	FDA UDI	Class II	Unknown
Knee-Lok Positioning Cushion	MTAKS01	FDA UDI	Class II	Unknown
Arm Support	MT40016	EUDAMEDFDA UDI	Class II	Active
IPPS Overlay	MTIL6460	FDA UDI	Class II	Unknown
Pronumbra	RT-C892K	EUDAMEDFDA UDI	Class II	Active
Posifix® -1 Baseplate	101019	EUDAMEDFDA UDI	Class II	Active
Respiratory Plate Cushion	BPL007	FDA UDI	Class II	Active
Solstice™ MR SRS Immobilization System	CHS03MR	EUDAMEDFDA UDI	Class II	Active
ProForm™ Thermoplastic	PRO330IM1832SG	EUDAMEDFDA UDI	Class II	Active
Monarch™ Individual Hand Grips	OAP160	FDA UDI	Class II	Unknown
Universal Couchtop™	MTIL604515	FDA UDI	Class II	Active
Type-S™ Thermoplastic	MTAPUD1224	EUDAMEDFDA UDI	Class II	Active
Patient Hand Grips	MTSBRT005	EUDAMEDFDA UDI	Class II	Active
Positioning Cushion	301205	EUDAMEDFDA UDI	Class II	Active
ThermFix Superior Bar	MTWBL002	FDA UDI	Class II	Active
Type-S™ Thermoplastic	MTAPUID1832	EUDAMEDFDA UDI	Class II	Active
IPPS Overlay	MTIL6003	FDA UDI	Class II	Unknown
Vac-Lok™ Cushion	VLPLV01C	EUDAMEDFDA UDI	Class II	Active

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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.