Data / Medical devices / United States / CQ Decimal, LLC

CQ Decimal, LLC: FDA-registered device maker in Sanford, FL, United States, 13 510(k) clearances

Name: CQ Decimal, LLC FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

CQ Decimal, LLC is registered with the FDA (registration 3003586672) in Sanford, FL, United States. It lists 3 device types. The FDA files 13 510(k) clearances under its listings, the newest dated July 1, 2021. Registered through 2026. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Get makers like this one Watch CQ Decimal, LLC

FDA registration number: 3003586672
Address: 121 Central Park Pl, Sanford, FL, United States, 32771
Owner or operator: Medtec LLC (9033077)
Roles: Manufacturer
First device listed: May 28, 2026
Registered through: 2026
Brand names listed: .DECIMAL ELECTRON APERTURE, .DECIMAL PHOTON BLOCK, .DECIMAL PROTON APERTURE, .DECIMAL RANGE COMPENSATOR, .Decimal Aperture, .Decimal Tissue Compensator/Intensity Modulator, .decimal Astroid Dosimetry App, .decimal p.d and more

Devices it lists

Device	Product code	Class	Role	Source
Accelerator, Linear, Medical	IYE	2	Manufacturer	accessdata.fda.gov
Block, Beam-Shaping, Radiation Therapy	IXI	2	Manufacturer	accessdata.fda.gov
System, Planning, Radiation Therapy Treatment	MUJ	2	Manufacturer	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
July 1, 2021	K211511	decimal Bolus	MUJ	Substantially Equivalent	.Decimal, LLC	accessdata.fda.gov
December 13, 2019	K192554	decimal3D	MUJ	Substantially Equivalent	.Decimal, LLC	accessdata.fda.gov
May 15, 2018	K173940	Astroid Planning App	MUJ	Substantially Equivalent	.Decimal, LLC	accessdata.fda.gov
August 7, 2015	K151369	.decimal p.d	MUJ	Substantially Equivalent	.Decimal, LLC	accessdata.fda.gov
May 15, 2015	K150547	.decimal Astroid Dosimetry App	MUJ	Substantially Equivalent	.Decimal, Inc.	accessdata.fda.gov
October 16, 2013	K132236	.DECIMAL PROTON APERTURE	IXI	Substantially Equivalent	.Decimal, Inc.	accessdata.fda.gov
November 21, 2012	K123015	.DECIMAL PHOTON BLOCK	IXI	Substantially Equivalent	.Decimal, Inc.	accessdata.fda.gov
September 9, 2011	K111759	.DECIMAL ELECTRON APERTURE	IXI	Substantially Equivalent	.Decimal, Inc.	accessdata.fda.gov
July 21, 2009	K091911	BOLUS COMPENSATOR	IXI	Substantially Equivalent	.Decimal, Inc.	accessdata.fda.gov
May 22, 2007	K071078	.DECIMAL RANGE COMPENSATOR	IXI	Substantially Equivalent	.Decimal, Inc.	accessdata.fda.gov
May 18, 2007	K071077	.DECIMAL APERTURE	IXI	Substantially Equivalent	.Decimal, Inc.	accessdata.fda.gov
April 28, 2004	K040804	.DECIMAL TISSUE COMPENSATOR/INTENSITY MODULATOR	IXI	Substantially Equivalent	Southeastern Radiation Products, Inc.	accessdata.fda.gov
November 22, 2002	K023636	BLOCKING TRAY	IYE	Substantially Equivalent	Southeastern Radiation Products, Inc.	accessdata.fda.gov

Compare with other makers

Updated July 1, 2021. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.