Data / Medical devices / United States / Jumar Corporation
Jumar Corporation: FDA-registered device maker in Bainbridge Is, WA, United States, 1 510(k) clearance
Jumar Corporation is registered with the FDA (registration 3015216243) in Bainbridge Is, WA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated August 12, 1983. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3015216243
- Address
- 9431 Coppertop Loop Rd NE Suite 101 Box 29 --, Bainbridge Is, WA, United States, 98110
- Owner or operator
- JUMAR CORPORATION (1420333)
- Roles
- Manufacturer
- First device listed
- December 3, 2007
- Registered through
- 2027
- Brand names listed
- Aqualizer Mouthpiece
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Positioner, Tooth, Preformed | KMY | 1 | Manufacturer | accessdata.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.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| August 12, 1983 | K831793 | AQUALIZER MOUTHPIECE | KMY | Substantially Equivalent | Martin D. Lerman | accessdata.fda.gov |
Compare with other makers
Updated August 12, 1983. 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.