Data / Medical devices / United States / Boone Center, Incorporated
Boone Center, Incorporated: FDA-registered device maker in Moscow Mills, MO, United States, 1 510(k) clearance
Boone Center, Incorporated is registered with the FDA (registration 1937639) in Moscow Mills, MO, United States. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated May 26, 1978. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1937639
- Address
- 245 College Campus Dr, Moscow Mills, MO, United States, 63362
- Owner or operator
- BOONE CENTER, INC. (1937639)
- Roles
- Repackager or relabeler
- First device listed
- December 10, 2013
- Registered through
- 2026
- Brand names listed
- Oyster Shell
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Detectors And Removers, Lice, (Including Combs) | LJL | 1 | Repackager or relabeler | accessdata.fda.gov |
| Evacuator, Oral Cavity | EHZ | 1 | Repackager or relabeler | accessdata.fda.gov |
| Handpiece, Contra- And Right-Angle Attachment, Dental | EGS | 1 | Repackager or relabeler | 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 |
|---|---|---|---|---|---|---|
| May 26, 1978 | K780752 | PROPHYLAXIS ANGLE | EGS | Substantially Equivalent | Young Dental Manufacturing Co. 1, LLC | accessdata.fda.gov |
Compare with other makers
- All makers of Handpiece, Contra- And Right-Angle Attachment, Dental
- All makers of Evacuator, Oral Cavity
- All makers of Detectors And Removers, Lice, (Including Combs)
Updated May 26, 1978. 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.