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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 16 of 22

Device	Model / Reference	Registries	Class	Status
Thorawedge™ Locator	TWI100	EUDAMEDFDA UDI	Class II	Active
trUpoint ARCH Replacement Kit	MTHF033	FDA UDI	Class II	Unknown
Shim	MTSHIM01	EUDAMEDFDA UDI	Class II	Active
IPPS™ Overlay	MTIL6420	FDA UDI	Class II	Active
Body Pro-Lok ONE™ System	BPL100	FDA UDI	Class II	Unknown
IPPS Overlay	MTIL4301	FDA UDI	Class II	Unknown
Vac-Lok™ Cushion	VLWGB03C	EUDAMEDFDA UDI	Class II	Active
IPPS™ Couchtop	MTIL6001	FDA UDI	Class II	Unknown
Uni-frame® Thermoplastic	MTAPUL	EUDAMEDFDA UDI	Class II	Active
Bolus	MTCB403S	FDA UDI	Class I	Unknown
Vac-Lok™ Cushion	VLPLV02	EUDAMEDFDA UDI	Class II	Active
Locators	662050	FDA UDI	Class II	Unknown
Guide Pins	109039	FDA UDI	Class II	Unknown
Solstat™ Immobilization System	CHS14	FDA UDI	Class II	Unknown
Rails-Only System	MTSBRT060	FDA UDI	Class II	Active
ProForm™ Pediatric Thermoplastic	PRO430IM1832	EUDAMEDFDA UDI	Class II	Active
Forehead Brace	MTSBRT018	FDA UDI	Class II	Active
Headrest	MTSILVER2B	EUDAMEDFDA UDI	Class II	Active
Thermoplastic Frame	MTSNT3	FDA UDI	Class II	Active
Interface for Varian	MTIL6612	FDA UDI	Class II	Active
C-Qual™	MT400	EUDAMEDFDA UDI	Class II	Active
Docking Station	MTIL3001103	FDA UDI	Class II	Unknown
Vac-Lok Cushion	MTVLARM02C	FDA UDI	Class II	Unknown
Chabner XRT Radiation Bra	CRTBRA05	FDA UDI	Class II	Unknown
Head Support	CHS42	EUDAMEDFDA UDI	Class II	Active
ProForm™ Head and Neck Extension	MTIL6680	FDA UDI	Class II	Active
Locators	109037	FDA UDI	Class II	Unknown
SnapFrame™ Type-S™ Thermoplastic	MTAPSDMP	FDA UDI	Class II	Unknown
Prodigy™ Lok-Bar™	MTIL3454	FDA UDI	Class II	Active
Posicast® Thermoplastic	920030	FDA UDI	Class II	Unknown
Positioning Cushion	301082	FDA UDI	Class II	Active
Uni-frame® Thermoplastic	MTAPUI2232	FDA UDI	Class II	Unknown
Thermoplastic	MTAPS18391	EUDAMEDFDA UDI	Class II	Active
Pediatric Cushion Guide	PRO450	EUDAMEDFDA UDI	Class II	Active
Positioning Cushion	301016	EUDAMEDFDA UDI	Class II	Active
Headrest	MTSILVER2C	EUDAMEDFDA UDI	Class II	Active
Lok-Bar™	MTVR1000	FDA UDI	Class II	Unknown
Shoulder Retractors	20SR02SUB3	EUDAMEDFDA UDI	Class II	Active
Pro Posifix® Headrest Adapter	OAP121	EUDAMEDFDA UDI	Class II	Active
Vac-Lok™ Cushion	VLG40	EUDAMEDFDA UDI	Class II	Active
IPPS™ Overlay	MTIL4000	FDA UDI	Class II	Unknown
Arm Support	106016	FDA UDI	Class II	Unknown
Vac-Lok™ Cushion	VLTYS02CX	EUDAMEDFDA UDI	Class II	Active
Type-S™ Variable Axis Baseplate	MTCFHNVAB01	EUDAMEDFDA UDI	Class II	Active
Headrest - Timo size C with base	MTTIMO2CL	EUDAMEDFDA UDI	Class II	Active
Type-S™ Lok-Bar™	MTWBL001	FDA UDI	Class II	Active
Couchtop Panel	MTIL3202	FDA UDI	Class II	Unknown
Solstice™ SRS Immobilization System	CHS03	EUDAMEDFDA UDI	Class II	Active
Palliative Grid Extension	MTIL6602	FDA UDI	Class II	Unknown
Vac-Lok™ Cushion	VL0008	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.