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Data / Medical devices / United States / Pharma Supply, Inc.

Pharma Supply, Inc.: FDA-registered device maker in Wellington, FL, United States, 14 510(k) clearances

Pharma Supply, Inc. is registered with the FDA (registration 1066444) in Wellington, FL, United States. It lists 11 device types. The FDA files 14 510(k) clearances under its listings, the newest dated November 22, 2023. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
1066444
FEI number
3003405786
Address
3361 Fairlane Farms RD., Wellington, FL, United States, 33414
Owner or operator
PHARMA SUPPLY, INC. (9046840)
Roles
Complaint file establishment
First device listed
December 28, 2018
Registered through
2026

Devices it lists

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
November 22, 2023K231797Medifun Lancing Device, Model No. LD-E1QRLSubstantially EquivalentMedifun Corporationaccessdata.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
January 5, 2021K193273Insulin SyringeFMFSubstantially EquivalentPromisemed Hangzhou Meditech Co., Ltd.accessdata.fda.gov
September 5, 2019K191004Advocate Non-Contact Infrared ThermometerFLLSubstantially EquivalentBroadmaster Biotech, Corp.accessdata.fda.gov
May 11, 2017K161950Common Type Insulin Pen Needle, Safety Type Insulin Pen NeedleFMISubstantially EquivalentPromisemed Hangzhou Meditech Co., Ltd.accessdata.fda.gov
October 19, 2016K160199Advocate Insulin Pen NeedlesFMISubstantially EquivalentDiabetic Supply of Suncoast, Inc.accessdata.fda.gov
April 17, 2015K150430Arm Blood Pressure Monitor, Wrist Blood Pressure MonitorDXNSubstantially EquivalentFudakang Industrial Co., Ltd.accessdata.fda.gov
May 11, 2012K120183ADVOCATE REDI-CODE+BMB-EA001S BLOOD GLUCOSE MONITORING SYSTEMNBWSubstantially EquivalentBroadmaster Biotech Corperationaccessdata.fda.gov
March 15, 2011K110018FULLY AUTOMATIC ELECTRONIC BLOOD PRESSURE MONITORDXNSubstantially EquivalentAndon Health Co, Ltd.accessdata.fda.gov
August 3, 2010K101387DIGITAL THERMOMETER, MODELS BT-A11CN, BT-A21CN, BT-A41CNFLLSubstantially EquivalentFudakang Industries Co., Ltd.accessdata.fda.gov
February 27, 2009K083395SEMI-FULLY AUTOMATIC ELECTRONIC BLOOD PRESSURE MONITOR, MODELS: KD-322,KD-622,KD-575,KD-525E,KD-593,KD-595,KD-596,KD-598DXNSubstantially EquivalentAndon Health Co, Ltd.accessdata.fda.gov
January 29, 2009K083248FULLY AUTOMATED ELECTRONIC BLOOD PRESSURE MONITOR, MODEL KD-7902DXNSubstantially EquivalentAndon Health Co, Ltd.accessdata.fda.gov
August 23, 2007K070988SC PROFI FINE PEN NEEDLE, MODELS; 5MM, 8MM, 12.7MM (28G, 29G, 30G, 31G)FMISubstantially EquivalentShinchang Medical Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated November 22, 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.