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Data / Medical devices / United States / Remington Medical, Inc.

Remington Medical, Inc.: FDA-registered device maker in Alpharetta, GA, United States, 7 510(k) clearances

Remington Medical, Inc. is registered with the FDA (registration 3007014520) in Alpharetta, GA, United States. It lists 33 device types. The FDA files 7 510(k) clearances under its listings, the newest dated November 20, 2025. Registered through 2026. FDA data exported November 3, 2026.

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Get makers like this oneWatch Remington Medical, Inc.
FDA registration number
3007014520
Address
6245 Shiloh Road Suite C, Alpharetta, GA, United States, 30005
Owner or operator
REMINGTON MEDICAL, INC. (9006473)
Roles
Contract manufacturer, Manufacturer, Manufacturer for export
First device listed
February 28, 2006
Registered through
2026
Brand names listed
301-CG Family, ADAP-1 Family, ADAP-2 Family, ADAP-2000 Family, ADAP-2R Family, ADAP-2RL Family, Adapter Cap, BS-101-97 Family and more

Devices it lists

DeviceProduct codeClassRoleSource
Appliance, Fixation, Spinal InterlaminalKWP2Contract manufactureraccessdata.fda.gov
Appliance, Fixation, Spinal Intervertebral BodyKWQ2Contract manufactureraccessdata.fda.gov
Bit, DrillHTW1Contract manufactureraccessdata.fda.gov
Bone Cement, Posterior Screw AugmentationPML2Contract manufactureraccessdata.fda.gov
Cable, ElectrodeIKD2Contract manufactureraccessdata.fda.gov
Cable, Transducer And Electrode, Patient, (Including Connector)DSA2Manufactureraccessdata.fda.gov
Catheter, SteerableDRA2Manufacturer for exportaccessdata.fda.gov
Cuff, Tracheal Tube, InflatableBSK2Contract manufactureraccessdata.fda.gov
Dispenser, Liquid MedicationKYX1Contract manufactureraccessdata.fda.gov
Electromyograph, DiagnosticIKN2Contract manufactureraccessdata.fda.gov
Electrosurgical, Cutting & Coagulation & AccessoriesGEI2Contract manufactureraccessdata.fda.gov
Flowmeter, Blood, CardiovascularDPW2Manufactureraccessdata.fda.gov
Instrument, BiopsyKNW2Manufactureraccessdata.fda.gov
Instrument, Ultrasonic SurgicalLFLUContract manufactureraccessdata.fda.gov
Intervertebral Fusion Device With Bone Graft, LumbarMAX2Contract manufactureraccessdata.fda.gov
Intervertebral Fusion Device With Bone Graft, ThoracicPHM2Contract manufactureraccessdata.fda.gov
Marker, SkinFZZ1Contract manufactureraccessdata.fda.gov
Neurological Stereotaxic InstrumentHAW2Contract manufactureraccessdata.fda.gov
Neurosurgical Nerve LocatorPDQ2Contract manufactureraccessdata.fda.gov
Orthopedic Manual Surgical InstrumentLXH1Contract manufactureraccessdata.fda.gov
Orthopedic Stereotaxic InstrumentOLO2Contract manufactureraccessdata.fda.gov
Orthosis, Spinal Pedicle FixationMNI2Contract manufactureraccessdata.fda.gov
Orthosis, Spondylolisthesis Spinal FixationMNH2Contract manufactureraccessdata.fda.gov
Retractor, FiberopticFDG1Contract manufactureraccessdata.fda.gov
Set, I.V. Fluid TransferLHI2Manufactureraccessdata.fda.gov
Spinal Vertebral Body Replacement Device - CervicalPLR2Contract manufactureraccessdata.fda.gov
Stimulator, Electrical, Evoked ResponseGWF2Contract manufactureraccessdata.fda.gov
Stimulator, NerveETN2Contract manufactureraccessdata.fda.gov
System, X-Ray, MammographicIZH2Manufactureraccessdata.fda.gov
Table, Operating-Room, Ac-PoweredFQO1Contract manufactureraccessdata.fda.gov
Tape And Bandage, AdhesiveKGX1Contract manufactureraccessdata.fda.gov
Thoracolumbosacral Pedicle Screw SystemNKB2Contract manufactureraccessdata.fda.gov
Tubes, Gastrointestinal (And Accessories)KNT2Contract manufactureraccessdata.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
November 20, 2025K251904VascuChek Kit, VascuChek Transceiver, VascuChek Clinical Probe, VascuChek Speaker Dock (VC-KIT-02, VC-TRX-02, VC-CP-01, VC-SD-01); VascuChek Kit, VascuChek Transceiver, VascuChek Surgical Probe, VascuChek Speaker Dock (VC-KIT-02, VC-TRX-02, VC-SP-01, VC-SD-01)DPWSubstantially EquivalentRemington Medical, Inc.accessdata.fda.gov
January 27, 2022K211589VascuChek Kit, VascuChek Transceiver, VascuChek Surgical Probe, VascuChek ChargerDPWSubstantially EquivalentRemington Medical, Inc.accessdata.fda.gov
October 7, 2021K212065VascuChek Kit, VascuChek Transceiver, VascuChek Clinical Probe, VascuChek ChargerDPWSubstantially EquivalentRemington Medical, Inc.accessdata.fda.gov
July 12, 2019K191315Remington Medical, Inc. Automatic Cutting Needle (NAC)KNWSubstantially EquivalentRemington Medical, Inc.accessdata.fda.gov
November 3, 1998K983621NEEDLE GUIDEIZHSubstantially EquivalentRemington Medical, Inc.accessdata.fda.gov
August 26, 1997K972134BAG DECANTERLHISubstantially EquivalentRemington Medical, Inc.accessdata.fda.gov
July 23, 1997K971968SAFE CONNECT SURGICAL CABLE (S-101-97/S-201-97/FL-601-97)DSASubstantially EquivalentRemington Medical, Inc.accessdata.fda.gov

Compare with other makers

Updated November 20, 2025. 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.