Data / Medical devices / Adaptor, Recreational / United States
FDA-registered makers of Adaptor, Recreational in the United States: 14 establishments
14 establishments in the United States are registered with the FDA to make Adaptor, Recreational (product code ILT). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Adaptor, Recreational
- Product code
- ILT
- Country
- United States
Makers of Adaptor, Recreational in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| All Quality & Services, Inc. | Garland, TX, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| ASP Global, LLC | Austell, GA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| DeVilbiss Healthcare LLC. | Somerset, PA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Iilabco LLC | Brea, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Implus Footcare LLC | Durham, NC, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| In-Step Mobility Products Corporation | Skokie, IL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Inovo Inc. | Lehigh Acres, FL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Myrava, LLC | Indianapolis, IN, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| North Coast Medical, Inc. | Morgan Hill, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Peak Degrees LLC | Southlake, TX, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Performance Health Supply, LLC. | Cedarburg, WI, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Richardson Products, Inc. | Frankfort, IL, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Theradapt Products Inc. | Ludington, MI, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tumble Forms, Inc. | Dolgeville, NY, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. 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.