Data / Medical devices / United States / Hanuri Distribution, Inc
Hanuri Distribution, Inc: FDA-registered device maker in Chatsworth, CA, United States, 2 510(k) clearances
Hanuri Distribution, Inc is registered with the FDA (registration 3007778244) in Chatsworth, CA, United States. It lists 3 device types. The FDA files 2 510(k) clearances under its listings, the newest dated October 21, 2020. Registered through 2027. 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
- 3007778244
- Address
- 9601 Owensmouth Ave Ste 8, Chatsworth, CA, United States, 91311
- Owner or operator
- Hanuri distribution, inc (10030065)
- Roles
- Manufacturer, Repackager or relabeler
- First device listed
- December 8, 2011
- Registered through
- 2027
- Brand names listed
- Powerpress Cupping Set, Powerpress Recovery Unit, Powerpress Unit
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Device, Pressure Applying | KNM | 1 | Repackager or relabeler | accessdata.fda.gov |
| Massager, Powered Inflatable Tube | IRP | 2 | Manufacturer | accessdata.fda.gov |
| Sleeve, Limb, Compressible | JOW | 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 |
|---|---|---|---|---|---|---|
| October 21, 2020 | K202044 | Powerpress Recovery Unit | IRP | Substantially Equivalent | Hanuri Distribution, Inc. | accessdata.fda.gov |
| November 9, 2011 | K110276 | POWERPRESS UNIT | JOW | Substantially Equivalent | Hanuri Distribution, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Device, Pressure Applying
- All makers of Massager, Powered Inflatable Tube
- All makers of Sleeve, Limb, Compressible
Updated October 21, 2020. 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.