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Data / Medical devices / United States / Kenad SG Medical, Inc.

Kenad SG Medical, Inc.: FDA-registered device maker in Bartlett, TN, United States, 4 510(k) clearances

Kenad SG Medical, Inc. is registered with the FDA (registration 1054236) in Bartlett, TN, United States. It lists 21 device types. The FDA files 4 510(k) clearances under its listings, the newest dated November 22, 1996. Registered through 2026. FDA data exported November 2, 2026.

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Get makers like this oneWatch Kenad SG Medical, Inc.
FDA registration number
1054236
FEI number
1000112881
Address
3110 Stage Post Dr Ste 123, Bartlett, TN, United States, 38133
Owner or operator
KENAD SG MEDICAL, INC. (9002807)
Roles
Contract manufacturer, Manufacturer, Repackager or relabeler
First device listed
June 1, 1991
Registered through
2026

Devices it lists

DeviceProduct codeClassRoleSource
Accessories, TractionILZ1Manufacturer, Repackager or relabeleraccessdata.fda.gov
Aid, TransferIKX1Manufactureraccessdata.fda.gov
Bandage, CastITG1Repackager or relabeleraccessdata.fda.gov
Bandage, ElasticFQM1Repackager or relabeleraccessdata.fda.gov
Binder, AbdominalFSD1Manufactureraccessdata.fda.gov
Cover, LimbIPM1Contract manufactureraccessdata.fda.gov
Joint, Ankle, External BraceITW1Manufacturer, Repackager or relabeleraccessdata.fda.gov
Joint, Hip, External BraceITS1Repackager or relabeleraccessdata.fda.gov
Joint, Knee, External BraceITQ1Manufacturer, Repackager or relabeleraccessdata.fda.gov
Orthosis, CervicalIQK1Manufacturer, Repackager or relabeleraccessdata.fda.gov
Orthosis, LumbarIQE1Manufacturer, Repackager or relabeleraccessdata.fda.gov
Orthosis, Lumbo-SacralIPY1Repackager or relabeleraccessdata.fda.gov
Orthosis, Rib Fracture, SoftIPX1Manufactureraccessdata.fda.gov
Restraint, ProtectiveFMQ1Manufactureraccessdata.fda.gov
Scissors, Orthopedic, SurgicalHRR1Repackager or relabeleraccessdata.fda.gov
Shoe, CastIPG1Repackager or relabeleraccessdata.fda.gov
Sling, ArmILI1Manufactureraccessdata.fda.gov
Splint, ClavicleIQJ1Manufactureraccessdata.fda.gov
Splint, Hand, And ComponentsILH1Manufacturer, Repackager or relabeleraccessdata.fda.gov
Support, ArmIOY1Manufacturer, Repackager or relabeleraccessdata.fda.gov
Tips And Pads, Cane, Crutch And WalkerINP1Repackager 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
November 22, 1996K963430PROTECTIVE RESTRAINT (VEST RESTRAINT)FMQSubstantially EquivalentKenad SG Medical, Inc.accessdata.fda.gov
November 22, 1996K963422PROTECTIVE RESTRAINT (PROTECTIVE MITT)FMQSubstantially EquivalentKenad SG Medical, Inc.accessdata.fda.gov
November 22, 1996K963421PROTECTIVE RESTRAINT (WAIST HOLDER)FMQSubstantially EquivalentKenad SG Medical, Inc.accessdata.fda.gov
October 2, 1996K962626PATIENT PROTECTIVE LIMBFMQSubstantially EquivalentKenad SG Medical, Inc.accessdata.fda.gov

Compare with other makers

Updated November 22, 1996. 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.