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Data / Medical devices / Canada / Rapid Aid Corp.

Rapid Aid Corp.: FDA-registered device maker in MISSISSAUGA Ontario, Canada, 3 510(k) clearances

Rapid Aid Corp. is registered with the FDA (registration 9710505) in MISSISSAUGA Ontario, Canada. It lists 6 device types. The FDA files 3 510(k) clearances under its listings, the newest dated July 24, 2017. Registered through 2026. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

FDA registration number
9710505
FEI number
3003339304
Address
4120a Sladeview Crescent, MISSISSAUGA Ontario, Canada, L5L5Z3
Owner or operator
Rapid Aid Corp. (10028086)
Roles
Complaint file establishment, Contract manufacturer, Exporter to the US, Foreign private label distributor, Manufacturer, Repackager or relabeler, Specification developer
First device listed
December 29, 2008
Registered through
2026
Brand names listed
35059 Instant Cold Pack, Achilles Pack, Adhesive backed thermal skin patches, Ankle Pack, Calf/Shin Pack, Cold Pocket, Cold Slipper, Dorsum Pack and more

Devices it lists

DeviceProduct codeClassRoleSource
Accessory, Surgical ApparelLYU1Complaint file establishment, Contract manufacturer, Manufacturer, Repackager or relabeler, Specification developeraccessdata.fda.gov
Adhesive Backed Thermal Skin PatchesOMW1Contract manufacturer, Exporter to the US, Foreign private label distributor, Manufacturer, Repackager or relabeleraccessdata.fda.gov
Bag, IceKYR1Complaint file establishment, Foreign private label distributor, Manufactureraccessdata.fda.gov
Infant Heel Warmer (Chemical Heat Pack)MPO1Complaint file establishment, Contract manufacturer, Exporter to the US, Foreign private label distributor, Manufactureraccessdata.fda.gov
Pack, Hot Or Cold, DisposableIMD1Complaint file establishment, Contract manufacturer, Exporter to the US, Foreign private label distributor, Manufactureraccessdata.fda.gov
Pack, Hot Or Cold, ReusableIME1Contract manufacturer, Exporter to the US, 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
July 24, 2017K163295Infant Transport Mattress Warmer with DiscIMDSubstantially EquivalentRapid Aid Corp.accessdata.fda.gov
May 27, 2015K150627Rapid Aid Instant Disposable Infant Heel WarmerMPOSubstantially EquivalentRapid Aid Corp.accessdata.fda.gov
May 3, 2004K040856RAPID AID INSTANT DISPOSABLE INFANT HEEL WARMERMPOSubstantially EquivalentRapid Aid , Ltd.accessdata.fda.gov

Compare with other makers

Updated July 24, 2017. 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.