Data / Medical devices / United States / Proactive Comfort, LLC
Proactive Comfort, LLC: FDA-registered device maker in Chantilly, VA, United States, 1 510(k) clearance
Proactive Comfort, LLC is registered with the FDA (registration 3021027216) in Chantilly, VA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated March 31, 2016. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3021027216
- Address
- 3901 Centerview Dr Ste L, Chantilly, VA, United States, 20151
- Owner or operator
- Proactive Comfort, LLC (10051973)
- Roles
- Specification developer
- First device listed
- May 26, 2016
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Wheelchair, Mechanical | IOR | 1 | Specification developer | 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 31, 2016 | K152021 | Pure Tilt | IOR | Substantially Equivalent | Proactive Comfort, LLC | accessdata.fda.gov |
Compare with other makers
Updated March 31, 2016. 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.