Data / Medical devices / United States / General Physiotherapy Ii LLC
General Physiotherapy Ii LLC: FDA-registered device maker in Saint Charles, MO, United States, 3 510(k) clearances
General Physiotherapy Ii LLC is registered with the FDA (registration 1937060) in Saint Charles, MO, United States. It lists 2 device types. The FDA files 3 510(k) clearances under its listings, the newest dated April 6, 1987. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1937060
- FEI number
- 1000147357
- Address
- 3683 New Town Blvd, Saint Charles, MO, United States, 63301
- Owner or operator
- General Physiotherapy II LLC (10092333)
- Roles
- Manufacturer
- First device listed
- December 24, 2024
- Registered through
- 2026
- Brand names listed
- 209, 210, 212, 214, 215, 216, 217, 222, 223,225,, 227,228,229, 230, 242, 250, 251, 252, 253, 331, Accessory Tray, Body Postioner Model, Disposable Covers Model, G5® ALCTM with accessories, G5® Cellutec® with accessories, G5® Contour® with accessories and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Massager, Therapeutic, Electric | ISA | 1 | Manufacturer | accessdata.fda.gov |
| Percussor, Powered-Electric | BYI | 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 |
|---|---|---|---|---|---|---|
| April 6, 1987 | K870939 | VIBRACARE | ISA | Substantially Equivalent | General Physiotherapy, Inc. | accessdata.fda.gov |
| January 23, 1986 | K855129 | NEOCUSSOR (MASSAGER, BATTERY) POWERED | BYI | Substantially Equivalent | General Physiotherapy, Inc. | accessdata.fda.gov |
| September 5, 1985 | K852944 | FLEXIMATIC MASSAGER | ISA | Substantially Equivalent | General Physiotherapy, Inc. | accessdata.fda.gov |
Compare with other makers
Updated April 6, 1987. 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.