Data / Medical devices / United States / Pottymd, LLC
Pottymd, LLC: FDA-registered device maker in Knoxville, TN, United States, 1 510(k) clearance
Pottymd, LLC is registered with the FDA (registration 3005739654) in Knoxville, TN, United States. It lists 4 device types. The FDA files 1 510(k) clearance under its listings, the newest dated February 2, 2023. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3005739654
- Address
- 6800 Baum Dr, Knoxville, TN, United States, 37919
- Owner or operator
- POTTYMD, LLC (9085639)
- Roles
- Specification developer
- First device listed
- April 10, 2006
- Registered through
- 2026
- Brand names listed
- WET DETECTIVE OR WET STOP WIRELESS, Wee SECURE, Wet-Stop Waterproof Mattress Cover, wee BELL Newborn Circumcision Device, wee MEDICAL
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Alarm, Conditioned Response Enuresis | KPN | 2 | Specification developer | accessdata.fda.gov |
| Clamp, Circumcision | HFX | 2 | Specification developer | accessdata.fda.gov |
| Cover, Mattress (Medical Purposes) | FMW | 1 | Specification developer | accessdata.fda.gov |
| Pediatric Position Holder | PRN | 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 |
|---|---|---|---|---|---|---|
| February 2, 2023 | K221356 | Wee Bell | HFX | Substantially Equivalent | Wee Medical | accessdata.fda.gov |
Compare with other makers
- All makers of Pediatric Position Holder
- All makers of Cover, Mattress (Medical Purposes)
- All makers of Clamp, Circumcision
- All makers of Alarm, Conditioned Response Enuresis
Updated February 2, 2023. 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.