Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3015216243

FEI Number

3015216243

Entity Name

JUMAR CORPORATION

City/State/Country

Bainbridge Is, WA, US

Establishment Address

9431 Coppertop Loop Rd NE Suite 101 Box 29, --, Bainbridge Is, WA 98110, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

JUMAR CORPORATION (Owner Number: 1420333)

Owner / Operator Contact Address

9431 Coppertop Loop Rd NE Suite 101 Box 29, --, Bainbridge Is, WA 98110, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K831793

PMA Number

N/A

All Registered Proprietary Names

Aqualizer Mouthpiece

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KMY	Positioner, Tooth, Preformed	Dental	Class 1	872.5525	2007-12-03

Official Correspondent

ROBERT LERMAN

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

JUMAR CORPORATION

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015216243. Last updated year: 2026. Please use registration number 3015216243 when referencing this establishment in official correspondence.