Data / Medical devices / United States / Velocity Orthopedics, Inc.
Velocity Orthopedics, Inc.: FDA-registered device maker in Rancho Cucamonga, CA, United States, 2 510(k) clearances
Velocity Orthopedics, Inc. is registered with the FDA (registration 3009147292) in Rancho Cucamonga, CA, United States. It lists 5 device types. The FDA files 2 510(k) clearances under its listings, the newest dated July 29, 2016. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3009147292
- Address
- 10700 Jersey Blvd Ste 360, Rancho Cucamonga, CA, United States, 91730
- Owner or operator
- Velocity Orthopedics, Inc. (10036951)
- Roles
- Manufacturer, Repackager or relabeler
- First device listed
- June 7, 2011
- Registered through
- 2026
- Brand names listed
- Velocity, Velox
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Blade, Saw, General & Plastic Surgery, Surgical | GFA | 1 | Manufacturer | accessdata.fda.gov |
| Bur, Surgical, General & Plastic Surgery | GFF | 1 | Manufacturer | accessdata.fda.gov |
| Electrosurgical, Cutting & Coagulation & Accessories | GEI | 2 | Repackager or relabeler | accessdata.fda.gov |
| Instrument, Manual, Surgical, General Use | MDM | 1 | Manufacturer | accessdata.fda.gov |
| Silicone Hydrogel For Scar Management | PFP | 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 |
|---|---|---|---|---|---|---|
| July 29, 2016 | K161558 | Bovie 3.3mm Disposable Bipolar Ablator 90°, Aspirating and Non-Aspirating, Bovie 2.4mm Disposable Bipolar Ablator 55°, Non-Aspirating, Bovie 1.8mm Disposable Bipolar Ablator 60°, Non-Aspirating | GEI | Substantially Equivalent | Bovie Medical Corporation | accessdata.fda.gov |
| January 15, 2016 | K152777 | Bovie Disposable Bipolar Ablator | GEI | Substantially Equivalent | Bovie Medical Corporation | accessdata.fda.gov |
Compare with other makers
- All makers of Blade, Saw, General & Plastic Surgery, Surgical
- All makers of Instrument, Manual, Surgical, General Use
- All makers of Electrosurgical, Cutting & Coagulation & Accessories
- All makers of Bur, Surgical, General & Plastic Surgery
- All makers of Silicone Hydrogel For Scar Management
Updated July 29, 2016. 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.