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Data / Medical devices / United States / Fora Care Inc.

Fora Care Inc.: FDA-registered device maker in Moorpark, CA, United States, 40 510(k) clearances

Fora Care Inc. is registered with the FDA (registration 3007134734) in Moorpark, CA, United States. It lists 21 device types. The FDA files 40 510(k) clearances under its listings, the newest dated December 19, 2023. Registered through 2027. FDA data exported November 2, 2026.

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FDA registration number
3007134734
Address
893 Patriot Dr Ste D, Moorpark, CA, United States, 93021
Owner or operator
Fora Care Inc. (10026431)
Roles
Complaint file establishment
First device listed
November 8, 2010
Registered through
2027
Brand names listed
FORA, FORA Control Solution, FORA Control Solution for ?-Ketone Test (L1), FORA Control Solution for ?-Ketone Test (L2), FORA Control Solution for Lactate Test (L1), FORA Control Solution for Total Cholesterol Test (L1), FORA Control Solution for Uric Acid Test (L1), FORA D10 Blood Glucose plus Blood Pressure Monitoring System and more

Devices it lists

DeviceProduct codeClassRoleSource
Acid, Lactic, Enzymatic MethodKHP1Complaint file establishmentaccessdata.fda.gov
Calculator/Data Processing Module, For Clinical UseJQP1Complaint file establishmentaccessdata.fda.gov
Continuous Measurement ThermometerFLL2Complaint file establishmentaccessdata.fda.gov
ElectrocardiographDPS2Complaint file establishmentaccessdata.fda.gov
Enzymatic Esterase--Oxidase, CholesterolCHH1Complaint file establishmentaccessdata.fda.gov
Glucose Dehydrogenase, GlucoseLFR2Complaint file establishmentaccessdata.fda.gov
Glucose Oxidase, GlucoseCGA2Complaint file establishmentaccessdata.fda.gov
Mask, SurgicalFXX2Complaint file establishmentaccessdata.fda.gov
Meter, Peak Flow, SpirometryBZH2Complaint file establishmentaccessdata.fda.gov
Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)MWI2Complaint file establishmentaccessdata.fda.gov
Multiple Use Blood Lancet For Single Patient Use OnlyQRL2Complaint file establishmentaccessdata.fda.gov
Nebulizer (Direct Patient Interface)CAF2Complaint file establishmentaccessdata.fda.gov
Nitroprusside, Ketones (Urinary, Non-Quant.)JIN1Complaint file establishmentaccessdata.fda.gov
OximeterDQA2Complaint file establishmentaccessdata.fda.gov
Scale, Stand-On, PatientFRI1Complaint file establishmentaccessdata.fda.gov
Single (Specified) Analyte Controls (Assayed And Unassayed)JJX1Complaint file establishmentaccessdata.fda.gov
Single Use Only Blood Lancet With An Integral Sharps Injury Prevention FeatureFMK2Complaint file establishmentaccessdata.fda.gov
Single Use Only Blood Lancet Without An Integral Sharps Injury Prevention FeatureQRK2Complaint file establishmentaccessdata.fda.gov
System, Measurement, Blood-Pressure, Non-InvasiveDXN2Complaint file establishmentaccessdata.fda.gov
System, Test, Blood Glucose, Over The CounterNBW2Complaint file establishmentaccessdata.fda.gov
Transmitters And Receivers, Physiological Signal, RadiofrequencyDRG2Complaint file establishmentaccessdata.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.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
December 19, 2023K222810TD-7301 Peak Flow meterBZHSubstantially EquivalentGostar Co., Ltd.accessdata.fda.gov
January 20, 2023K221419TD-5010 Lancing Device and TD-5084 Sterile LancetsQRLSubstantially EquivalentGostar Co., Ltd.accessdata.fda.gov
October 28, 2022K221521Disposable Safety LancetFMKSubstantially EquivalentSteriLance Medical (Suzhou), Inc.accessdata.fda.gov
July 6, 2022K220475Lancet (I, II, III, V, VI); Lancing device (HH-X-T, HH-XIII-T, HH-XV-T, HH-XVI-T, HH-XVII-T, HH-XVIII-T, HH-XIX, HH-XXI-T, HH-XXII-T, HH-XXIII-T, HH-XXIV-T)QRLSubstantially EquivalentTianjin Huahong Technology Co., Ltd.accessdata.fda.gov
May 19, 2022K220370Safety Lancet (XIII, XVII, XXI, XXII, XXIII, XXIV, XXV, XXVI)FMKSubstantially EquivalentTianjin Huahong Technology Co., Ltd.accessdata.fda.gov
August 26, 2020K201549Motex Anti-Fog Surgical Face MaskFXXSubstantially EquivalentModern Healthcare Corp.accessdata.fda.gov
August 9, 2018K173505FORA GTel Blood Glucose Monitoring SystemNBWSubstantially EquivalentForacare, Inc.accessdata.fda.gov
November 10, 2016K161738FORA ADVANCED GD40 and FORA ADVANCED GD40 pro Blood Glucose and ß-Ketone Monitoring SystemsNBWSubstantially EquivalentTaidoc Technology Corporationaccessdata.fda.gov
March 2, 2016K151024Finger Type Pulse OximeterDQASubstantially EquivalentTaidoc Technology Corporationaccessdata.fda.gov
April 25, 2014K133588FORA CARE BLOOD PRESSURE MONITORING SYSTEMDXNSubstantially EquivalentForacare, Inc.accessdata.fda.gov
March 21, 2013K122060CLEVER TD-7001NEBULIZERCAFSubstantially EquivalentTaidoc Technology Corporationaccessdata.fda.gov
February 6, 2012K111890FORA DIAMOND PRIMA BLOOD GLUCOSE MONITORING SYSTEM, FORA DIAMOND MINI BLOOD GLUCOSE MONITORING SYSTEMNBWSubstantially EquivalentTaidoc Technology Corporationaccessdata.fda.gov
December 21, 2011K112274U-RIGHT TD-3135 BLOOD PRESSURE MONITORING SYSTEMDXNSubstantially EquivalentTaidoc Technology Corporationaccessdata.fda.gov
December 20, 2011K101926FORA D40 BLOOD GLUCOSE PLUS BLOOD PRESSURE MONITORING SYSTEMNBWSubstantially EquivalentTaidoc Technology Corporationaccessdata.fda.gov
December 15, 2011K112275FORA PREMIUM V10 BLOOD GLUCOSE MONITORING SYSTEMNBWSubstantially EquivalentTaidoc Technology Corporationaccessdata.fda.gov
July 7, 2011K110044FORA P30 PLUS MULTI-MODE BLOOD PRESSURE MONITORING SYSTEMDXNSubstantially EquivalentForacare, Inc.accessdata.fda.gov
July 6, 2011K092688FORA POCT S10/TD-4258 BLOOD GLUCOSE MONITORING SYSTEMLFRSubstantially EquivalentTaidoc Technology Corporationaccessdata.fda.gov
July 1, 2011K111029FORA POCT MANAGMENT SYSTEMNBWSubstantially EquivalentTaidoc Technology Corporationaccessdata.fda.gov
June 27, 2011K101509U-RIGHT TD-4279 BLOOD GLUCOSE MONITORING SYSTEM, FORA GD40/TD-4272 BLOOD GLUCOSE MONITORING SYSTEMNBWSubstantially EquivalentTaidoc Technology Corporationaccessdata.fda.gov
May 13, 2011K110948HEALTH CARE SYSTEM SOFTWARENBWSubstantially EquivalentTaidoc Technology Corporationaccessdata.fda.gov
March 1, 2011K101569V-TRUST MODEL TD-2202 PORTABLE ECG RECORDERDPSSubstantially EquivalentTaidoc Technology Corporationaccessdata.fda.gov
December 15, 2010K101012V-TRUST HANDHELD PULSE OXIMETER MODEL: TD-8201DQASubstantially EquivalentTaidoc Technology Corporationaccessdata.fda.gov
July 29, 2010K093724FORA CONTROL SOLUTION, TAIDOC CONTROL SOLUTIONJJXSubstantially EquivalentTaidoc Technology Corporationaccessdata.fda.gov
July 9, 2010K100732FORA G30A BLOOD GLUCOSE MONITORING SYSTEM, MODEL TD-4241NBWSubstantially EquivalentTaidoc Technology Corporationaccessdata.fda.gov
July 9, 2010K100405FORA G90 PERFORM BLOOD GLUCOSE MONITORING SYSTEMCGASubstantially EquivalentTaidoc Technology Corporationaccessdata.fda.gov
June 28, 2010K100322TD-4277 BLOOD GLUCOSE MONITORING SYSTEM, MODEL 4277NBWSubstantially EquivalentTaidoc Technology Corporationaccessdata.fda.gov
June 17, 2010K101259V-TRUST TD-8002 MULTI-PARAMETER SPOT-CHECK MONITOR MODEL TD-8002MWISubstantially EquivalentTaidoc Technology Corporationaccessdata.fda.gov
May 5, 2010K094005FORA G31A/TD-4256A BLOOD GLUCOSE MONITORING SYSTEM AND FORA G31B/TD-4256B BLOOD GLUCOSE MONITORING SYSTEMNBWSubstantially EquivalentTaidoc Technology Corporationaccessdata.fda.gov
February 19, 2010K093712FORA G71A BLOOD GLUCOSE MONITORING SYSTEM, TD-4274 BLOOD GLUCOSE MONITORING SYSTEMNBWSubstantially EquivalentTaidoc Technology Corporationaccessdata.fda.gov
February 18, 2010K093635MODELS FORA V30 AND TD-4242 BLOOD GLUCOSE MONITORING SYSTEMSNBWSubstantially EquivalentTaidoc Technology Corporationaccessdata.fda.gov
February 5, 2010K093005FORA G72 BLODO GLUCOSE MONITORING SYSTEM/TD-4264 BLOOD GLUCOSE MONITORING SYSTEM, MODEL TD-4264NBWSubstantially EquivalentTaidoc Technology Corporationaccessdata.fda.gov
January 25, 2010K092106U-RIGHT TD-3132 BLOOD PRESSURE MONITOR, FORA P 20 BLOOD PRESSURE MONITOR, MODEL TD-3132, TD-3132DXNSubstantially EquivalentTaidoc Technology Corporationaccessdata.fda.gov
December 24, 2009K093035FORA V10 BLOOD GLUCOSE MONITORING SYSTEM, MODEL TD-4244NBWSubstantially EquivalentTaidoc Technology Corporationaccessdata.fda.gov
December 10, 2009K092099NO-CODING BLOOD GLUCOSE MONITORING SYSTEM, MODELS TD-4251, TD-4252, TD-4253 AND TD-4254NBWSubstantially EquivalentTaidoc Technology Corporationaccessdata.fda.gov
November 20, 2009K091814FORA D20 BLOOD GLUCOSE PLUS BLOOD PRESSURE MONITORING SYSTEM; TD-3263 BLOOD GLUCOSE PLUS BLOOD PRESSURE MONITORING SYSTECGASubstantially EquivalentTaidoc Technology Corporationaccessdata.fda.gov
August 25, 2009K091897BLOOD PRESSURE MONITOR, MODEL FORA P11/TD-3019DXNSubstantially EquivalentTaidoc Technology Corporationaccessdata.fda.gov
May 12, 2009K090187FORA G30 BLOOD GLUCOSE MONITORING SYSTEM, MODEL TD-4241NBWSubstantially EquivalentTaidoc Technology Corporationaccessdata.fda.gov
March 26, 2009K090536FORA V12 NO-CODING BLOOD GLUCOSE MONITORING SYSTEM, MODEL TD-4247NBWSubstantially EquivalentTaidoc Technology Corporationaccessdata.fda.gov
January 16, 2009K083046FORA TELEHEALTH SYSTEMDRGSubstantially EquivalentTaidoc Technology Corporationaccessdata.fda.gov
July 25, 2008K081714FORA TD-3224 BLOOD GLUCOSE PLUS BLOOD PRESSURE MONITORING SYSTEMCGASubstantially EquivalentTaidoc Technology Corporationaccessdata.fda.gov

Compare with other makers

Updated December 19, 2023. 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.