Data / Medical devices / Australia / Riancorp Pty Ltd
Riancorp Pty Ltd: FDA-registered device maker in Henley Beach South Australia, Australia, 1 510(k) clearance
Riancorp Pty Ltd is registered with the FDA (registration 3006738449) in Henley Beach South Australia, Australia. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated December 23, 2004. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3006738449
- Address
- 2 331 Seaview Rd Henley Beach, Henley Beach South Australia, Australia, 5022
- Owner or operator
- RIANCORP PTY LTD (9098322)
- Roles
- Complaint file establishment, Specification developer
- First device listed
- February 28, 2007
- Registered through
- 2026
- Brand names listed
- LTU-904
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Light, Lymphedema Reduction, Low Energy | NZY | 2 | Complaint file establishment, Specification developer | 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 |
|---|---|---|---|---|---|---|
| December 23, 2004 | K030295 | LTU-904 PORTABLE LASER THERAPY UNIT | NZY | Substantially Equivalent | Riancorp Pty, Ltd. | accessdata.fda.gov |
Updated December 23, 2004. 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.