FDA.reportPublic FDA data

JUMAR CORPORATION

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30152162433015216243JUMAR CORPORATION1N2026-01-019431 Coppertop Loop Rd NE Suite 101 Box 29 -- Bainbridge Is WA US 98110

GUDID Contact Samples#

Sampled from matched GUDID device records for this company; this is not an exhaustive company contact directory.

Source GUDID, Product, Phone table
Source GUDIDProductPhoneEmail
00860013921101Aqualizer - Hydrostatic occlusal splint, Aqualizer assembly, Ultra Medium800-435-7863info@aqualizer.com
00860013921118Aqualizer - Hydrostatic occlusal splint, Aqualizer assembly, Ultra High800-435-7863info@aqualizer.com
00860013921132Aqualizer - Hydrostatic occlusal splint, Aqualizer assembly, Slim Medium800-435-7863info@aqualizer.com
00860013921149Aqualizer - Hydrostatic occlusal splint, Aqualizer assembly, Slim High800-435-7863info@aqualizer.com
00860013921156Aqualizer - Hydrostatic occlusal splint, Aqualizer assembly, Slim Low800-435-7863info@aqualizer.com
00860013921163Aqualizer - Hydrostatic occlusal splint, Aqualizer assembly, Mini Medium800-435-7863info@aqualizer.com
00860013921170Aqualizer - Hydrostatic occlusal splint, Aqualizer assembly, Mini High800-435-7863info@aqualizer.com
00860013921187Aqualizer - Hydrostatic occlusal splint, Aqualizer assembly, Mini Low800-435-7863info@aqualizer.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
2250112073050712K831793AQUALIZER MOUTHPIECEKMY1983-08-12

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
KMY11983-08-12

GUDID#