Data / Medical devices / United States / Dravon Medical, Inc.
Dravon Medical, Inc.: FDA-registered device maker in Clackamas, OR, United States, 1 510(k) clearance
Dravon Medical, Inc. is registered with the FDA (registration 3021643) in Clackamas, OR, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated September 26, 1983. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3021643
- Address
- 11465 SE Highway 212, Clackamas, OR, United States, 97015
- Owner or operator
- DRAVON MEDICAL INC. (9930031)
- Roles
- Manufacturer
- First device listed
- September 2, 1992
- Registered through
- 2026
- Brand names listed
- BLUE T-CLAMP, TRUE BLUE CLAMP
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Clamp | HXD | 1 | Manufacturer | accessdata.fda.gov |
| Instrument, Surgical, Disposable | KDC | 1 | 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 |
|---|---|---|---|---|---|---|
| September 26, 1983 | K831842 | DRAVON T CLAMP | KDC | Substantially Equivalent | Dravon Medical, Inc. | accessdata.fda.gov |
Compare with other makers
Updated September 26, 1983. 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.