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Data / Medical devices / United States / Precision Medical Devices Inc

Precision Medical Devices Inc: FDA-registered device maker in New Brunswick, NJ, United States, 1 510(k) clearance

Precision Medical Devices Inc is registered with the FDA (registration 3007478714) in New Brunswick, NJ, United States. It lists 20 device types. The FDA files 1 510(k) clearance under its listings, the newest dated August 7, 2020. Registered through 2026. FDA data exported November 2, 2026.

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Get makers like this oneWatch Precision Medical Devices Inc
FDA registration number
3007478714
Address
121 Jersey Ave Suite 203, New Brunswick, NJ, United States, 08901
Owner or operator
Precision Medical Devices (9098188)
Roles
Manufacturer, Repackager or relabeler, Specification developer
First device listed
December 10, 2009
Registered through
2026
Brand names listed
10ml Conical Bottom Self Standing Transport Tubes with Caps. Tubes are STERILE with tubes and caps PRE-attached, 10ml Conical Bottom Self Standing Transport Tubes with Caps. Tubes are STERILE with tubes and caps unattached., 10ml Conical Bottom Self Standing Transport Tubes with Caps. Tubes are non-sterile with tubes and caps not attached., 10ml Conical Bottom Self Standing Transport Tubes without Caps. Tubes are non-sterile with tubes and caps not attached., 3% Glutaraldehyde, Vial, CURETTES DERMAL 2MM, CURETTES DERMAL 3MM, CURETTES DERMAL 4MM and more

Devices it lists

DeviceProduct codeClassRoleSource
Blade, ScalpelGES1Repackager or relabeleraccessdata.fda.gov
Blood Collection Device For Cell-Free Nucleic AcidQMA2Repackager or relabeleraccessdata.fda.gov
Cassettes, TissueIDZ1Repackager or relabeleraccessdata.fda.gov
Clamp, Surgical, General & Plastic SurgeryGDJ1Repackager or relabeler, Specification developeraccessdata.fda.gov
Collector, Urine, (And Accessories) For Indwelling CatheterKNX2Repackager or relabeleraccessdata.fda.gov
Container, Specimen Mailer And Storage, Non-SterileNNK1Repackager or relabeleraccessdata.fda.gov
Container, Specimen, Non-SterileNNI1Specification developeraccessdata.fda.gov
Container, Specimen, SterileFMH1Specification developeraccessdata.fda.gov
Culture Media, Non-Selective And Non-DifferentialJSG1Repackager or relabeler, Specification developeraccessdata.fda.gov
Curette, EarJYG1Repackager or relabeleraccessdata.fda.gov
Dish, Tissue CultureKIZ1Repackager or relabeleraccessdata.fda.gov
Forceps, General & Plastic SurgeryGEN1Repackager or relabeleraccessdata.fda.gov
Formalin, Neutral BufferedIFP1Manufactureraccessdata.fda.gov
GlutaraldehydeIFT1Repackager or relabeleraccessdata.fda.gov
Instrument, Manual, Surgical, General UseMDM1Repackager or relabeler, Specification developeraccessdata.fda.gov
Kit, Screening, UrineJXA1Repackager or relabeleraccessdata.fda.gov
Punch, SurgicalLRY1Repackager or relabeleraccessdata.fda.gov
Scissors, General, SurgicalLRW1Repackager or relabeleraccessdata.fda.gov
Slides, MicroscopeKEW1Repackager or relabeleraccessdata.fda.gov
Tourniquet, PneumaticKCY1Repackager or relabeleraccessdata.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
August 7, 2020DEN200001Cell-Free DNA BCTQMAUnknownStreck, Inc.accessdata.fda.gov

Compare with other makers

Updated August 7, 2020. 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.