Data / Medical devices / United States / Slater Endoscopy, LLC
Slater Endoscopy, LLC: FDA-registered device maker in Miramar, FL, United States, 1 510(k) clearance
Slater Endoscopy, LLC is registered with the FDA (registration 3011099779) in Miramar, FL, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated June 8, 2015. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3011099779
- Address
- 10306 USA Today Way, Miramar, FL, United States, 33025
- Owner or operator
- Slater Endoscopy, LLC (10047312)
- Roles
- Manufacturer
- First device listed
- December 27, 2016
- Registered through
- 2026
- Brand names listed
- ENSIZOR
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Endoscopic Grasping/Cutting Instrument, Non-Powered | OCZ | 2 | 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 |
|---|---|---|---|---|---|---|
| June 8, 2015 | K150939 | Ensizor Endoscopic Scissors | OCZ | Substantially Equivalent | Slater Endoscopy, LLC | accessdata.fda.gov |
Compare with other makers
Updated June 8, 2015. 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.