Data / Medical devices / United States / Health-Mor, Inc
Health-Mor, Inc: FDA-registered device maker in Brooklyn, OH, United States, 2 510(k) clearances
Health-Mor, Inc is registered with the FDA (registration 3003007759) in Brooklyn, OH, United States. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated March 28, 2001. 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
- 3003007759
- Address
- 1 American Way Suite 1250, Brooklyn, OH, United States, 44144
- Owner or operator
- Health-Mor, Inc. (9044070)
- Roles
- Manufacturer
- First device listed
- April 22, 2013
- Registered through
- 2026
- Brand names listed
- Defender, Filter Queen
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Cleaner, Air, Medical Recirculating | FRF | 2 | 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 |
|---|---|---|---|---|---|---|
| March 28, 2001 | K010616 | DEFENDER ROOM AIR CLEANER, MODEL RAC-4000A | FRF | Substantially Equivalent | Hmi Industries, Inc. | accessdata.fda.gov |
| November 17, 2000 | K002692 | DEFENDER ROOM AIR CLEANER, MODEL RAC-3000A | FRF | Substantially Equivalent | Hmi Industries, Inc. | accessdata.fda.gov |
Compare with other makers
Updated March 28, 2001. 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.