Data / Medical devices / United States / Ortho-Cycle Co.
Ortho-Cycle Co.: FDA-registered device maker in Hollywood, FL, United States, 1 510(k) clearance
Ortho-Cycle Co. is registered with the FDA (registration 1052235) in Hollywood, FL, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated November 27, 1991. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1052235
- Address
- 2026 Scott St, Hollywood, FL, United States, 33020
- Owner or operator
- ORTHO-CYCLE CO. (1052235)
- Roles
- Reprocessor
- First device listed
- June 20, 2012
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Bracket, Metal, Orthodontic | EJF | 1 | Reprocessor | 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 |
|---|---|---|---|---|---|---|
| November 27, 1991 | K913913 | REFURBISHED ORTHODONTIC APPLIANCES | EJF | Substantially Equivalent | Ortho-Cycle Co. | accessdata.fda.gov |
Compare with other makers
Updated November 27, 1991. 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.