Data / Medical devices / United States / Deep Blue Medical Advances, Inc.
Deep Blue Medical Advances, Inc.: FDA-registered device maker in Durham, NC, United States, 1 510(k) clearance
Deep Blue Medical Advances, Inc. is registered with the FDA (registration 3017492634) in Durham, NC, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated March 30, 2020. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3017492634
- Address
- 701 W Main Street Suite 410, Durham, NC, United States, 27701
- Owner or operator
- Deep Blue Medical Advances, Inc. (10078119)
- Roles
- Specification developer
- First device listed
- October 11, 2020
- Registered through
- 2026
- Brand names listed
- T-Line Hernia Mesh
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Mesh, Surgical, Polymeric | FTL | 2 | 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 |
|---|---|---|---|---|---|---|
| March 30, 2020 | K193144 | T-Line Hernia Mesh | FTL | Substantially Equivalent | Deep Blue Medical Advances, Inc. | accessdata.fda.gov |
Compare with other makers
Updated March 30, 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.