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Data / Medical devices / Samoa / Mass Corporation

Mass Corporation: FDA-registered device maker in Apia Tuamasaga, Samoa, 1 510(k) clearance

Mass Corporation is registered with the FDA (registration 3010394125) in Apia Tuamasaga, Samoa. It lists 29 device types. The FDA files 1 510(k) clearance under its listings, the newest dated March 1, 2007. Registered through 2026. FDA data exported November 2, 2026.

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Get makers like this oneWatch Mass Corporation
FDA registration number
3010394125
Address
Offshore Chambers, P.O. Box 217, Apia, Apia Tuamasaga, Samoa, 22199
Owner or operator
Mass Corporation (10044726)
Roles
Exporter to the US
First device listed
July 19, 2013
Registered through
2026
Brand names listed
ACCESSORIES, WHEELCHAIR, ADAPTOR, GROOMING, ADAPTOR, HOLDER, SYRINGE, ADAPTOR, HYGIENE, APPARATUS, TRACTION, NON-POWERED, BED, MANUAL, BED, PATIENT ROTATION, MANUAL, CANE and more

Devices it lists

DeviceProduct codeClassRoleSource
Accessories, WheelchairKNO1Exporter to the USaccessdata.fda.gov
Adaptor, GroomingILW1Exporter to the USaccessdata.fda.gov
Adaptor, Holder, SyringeIQG1Exporter to the USaccessdata.fda.gov
Adaptor, HygieneILS1Exporter to the USaccessdata.fda.gov
Apparatus, Traction, Non-PoweredHST1Exporter to the USaccessdata.fda.gov
Bed, ManualFNJ1Exporter to the USaccessdata.fda.gov
Bed, Patient Rotation, ManualINY1Exporter to the USaccessdata.fda.gov
CaneIPS1Exporter to the USaccessdata.fda.gov
Cart, Emergency, Cardiopulmonary (Excluding Equipment)BZN1Exporter to the USaccessdata.fda.gov
Chair And Table, MedicalKMN1Exporter to the USaccessdata.fda.gov
Chair, Adjustable, MechanicalINN1Exporter to the USaccessdata.fda.gov
Chair, With CastersINM1Exporter to the USaccessdata.fda.gov
Components, WheelchairKNN1Exporter to the USaccessdata.fda.gov
CrutchIPR1Exporter to the USaccessdata.fda.gov
Cushion, FlotationKIC1Exporter to the USaccessdata.fda.gov
Exerciser, Non-MeasuringION1Exporter to the USaccessdata.fda.gov
Lift, Patient, Ac-PoweredFNG2Exporter to the USaccessdata.fda.gov
Mattress, Air Flotation, Alternating PressureFNM2Exporter to the USaccessdata.fda.gov
Mattress, Flotation Therapy, Non-PoweredIKY1Exporter to the USaccessdata.fda.gov
Monitor, Bed PatientKMI1Exporter to the USaccessdata.fda.gov
Orthosis, Corrective ShoeKNP1Exporter to the USaccessdata.fda.gov
Regulator, Pressure, Gas CylinderCAN1Exporter to the USaccessdata.fda.gov
Scale, Platform, WheelchairINF1Exporter to the USaccessdata.fda.gov
Stand, InfusionFOX1Exporter to the USaccessdata.fda.gov
Strap, Head, Gas MaskBTK1Exporter to the USaccessdata.fda.gov
Tips And Pads, Cane, Crutch And WalkerINP1Exporter to the USaccessdata.fda.gov
Walker, MechanicalITJ1Exporter to the USaccessdata.fda.gov
Walker, Mechanical, Poly Vinyl Chloride (Pvc)NXE1Exporter to the USaccessdata.fda.gov
Wheelchair, MechanicalIOR1Exporter to the USaccessdata.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
March 1, 2007K070176MAXHEALTH MECHANICAL WHEELCHAIR, K1IORSubstantially EquivalentMaxhealth Corp.accessdata.fda.gov

Compare with other makers

Updated March 1, 2007. 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.