Data / Medical devices / United States / Tiller Mind Body, Inc.
Tiller Mind Body, Inc.: FDA-registered device maker in San Antonio, TX, United States, 2 510(k) clearances
Tiller Mind Body, Inc. is registered with the FDA (registration 1648139) in San Antonio, TX, United States. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated August 29, 1996. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1648139
- FEI number
- 1000516428
- Address
- 10911 West Ave, San Antonio, TX, United States, 78213
- Owner or operator
- TILLER MIND BODY, INC. (9011577)
- Roles
- Complaint file establishment, Manufacturer, Specification developer
- First device listed
- March 19, 2008
- Registered through
- 2026
- Brand names listed
- Colonic Irrigation Devices, LIBBE Colon Hydrotherapy System, LIBBE Colon Hydrotherapy-Lower Bowel Evacuation System, LIBBE Colonic Irrigation System
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Colonic Irrigation System | KPL | 2 | Complaint file establishment, Manufacturer, 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 |
|---|---|---|---|---|---|---|
| August 29, 1996 | K962259 | LIBBE RECTAL TUBE (FORMERLY A YANKAUER SUCTION TUBE) | KPL | Substantially Equivalent | Tiller Mind Body, Inc. | accessdata.fda.gov |
| October 12, 1995 | K941279 | LOWER BOWEL EVACUATION SYSTEM | KPL | Substantially Equivalent | Tiller Mind Body, Inc. | accessdata.fda.gov |
Compare with other makers
Updated August 29, 1996. 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.