Data / Medical devices / United States / Protech Professional Products, Inc.
Protech Professional Products, Inc.: FDA-registered device maker in Boynton Beach, FL, United States, 1 510(k) clearance
Protech Professional Products, Inc. is registered with the FDA (registration 2435952) in Boynton Beach, FL, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated July 12, 2013. Registered through 2026. 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
- 2435952
- FEI number
- 1000137415
- Address
- 2900 Commerce Park Dr Ste 10, Boynton Beach, FL, United States, 33426
- Owner or operator
- PROTECH PROFESSIONAL PRODUCTS, INC. (9006187)
- Roles
- Manufacturer, Repackager or relabeler
- First device listed
- September 15, 2003
- Registered through
- 2026
- Brand names listed
- PROTECH CONCENTRAT, ProTech Plus Self Cure Hard Reline and Repair Acrylic, ProTech UBAR Metal Bonding Acrylic, SMILE AGAIN
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Cleanser, Denture, Over The Counter | EFT | 1 | Manufacturer | accessdata.fda.gov |
| Resin, Denture, Relining, Repairing, Rebasing | EBI | 2 | 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 |
|---|---|---|---|---|---|---|
| July 12, 2013 | K131036 | YAMAHACHI DENTURE BASE RESINS | EBI | Substantially Equivalent | Yamahachi Dental Manufacturing Co. | accessdata.fda.gov |
Compare with other makers
- All makers of Cleanser, Denture, Over The Counter
- All makers of Resin, Denture, Relining, Repairing, Rebasing
Updated July 12, 2013. 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.