Data / Medical devices / United States / Diversified Healthcare Development LLC.
Diversified Healthcare Development LLC.: FDA-registered device maker in Independence, VA, United States, 2 510(k) clearances
Diversified Healthcare Development LLC. is registered with the FDA (registration 3001541016) in Independence, VA, United States. It lists 3 device types. The FDA files 2 510(k) clearances under its listings, the newest dated April 18, 2007. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3001541016
- Address
- 60 Corporate Ln, Independence, VA, United States, 24348
- Owner or operator
- Diversified Healthcare Development, LLC. (10047697)
- Roles
- Manufacturer
- First device listed
- December 7, 2012
- Registered through
- 2026
- Brand names listed
- Drive, Korebalance, Koresway, ProBalance360
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Apparatus, Vestibular Analysis | LXV | U | Manufacturer | accessdata.fda.gov |
| Bottle, Collection, Vacuum | KDQ | 2 | Manufacturer | accessdata.fda.gov |
| Platform, Force-Measuring | KHX | 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 |
|---|---|---|---|---|---|---|
| April 18, 2007 | K070676 | KOREBALANCE (KINESTHETIC ABILITY TRAINER) | LXV | Substantially Equivalent | Sportkat, LLC | accessdata.fda.gov |
| November 19, 1991 | K911795 | KINESTHETIC ABILITY TRAINER (K.A.T., MODEL 1000) | LXV | Substantially Equivalent | Breg, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Bottle, Collection, Vacuum
- All makers of Apparatus, Vestibular Analysis
- All makers of Platform, Force-Measuring
Updated April 18, 2007. 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.