Data / Medical devices / United States / Perio Protect LLC
Perio Protect LLC: FDA-registered device maker in Saint Louis, MO, United States, 1 510(k) clearance
Perio Protect LLC is registered with the FDA (registration 3005167547) in Saint Louis, MO, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated January 23, 2004. Registered through 2027. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3005167547
- Address
- 9701 Green Park Industrial Dr, Saint Louis, MO, United States, 63123
- Owner or operator
- PERIO PROTECT LLC (9056881)
- Roles
- Manufacturer
- First device listed
- May 11, 2005
- Registered through
- 2027
- Brand names listed
- Perio Tray
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Tray, Fluoride, Disposable | KMT | 1 | 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 |
|---|---|---|---|---|---|---|
| January 23, 2004 | K031809 | PERIO PROTECT TRAY | KMT | Substantially Equivalent | Perio Protect, LLC | accessdata.fda.gov |
Compare with other makers
Updated January 23, 2004. 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.