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# FDA Clears T-Line Hernia Mesh
- URL: https://www.fdaweb.com/fda-clears-t-line-hernia-mesh/
- Published: 2020-08-13T12:00:00.000Z
- Updated: 2026-09-14T16:24:54.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5147428

FDA has cleared Deep Blue Medical Advances’ 510(k) for its T-Line hernia mesh with integrated suture-like extensions. The company [says](https://www.deepbluemedical.com/news-and-events?ref=fdaweb.com) the product provides superior anchoring strength and eliminates a key point of failure for conventional mesh fixation — the mesh/suture/tissue interface.

Deep Blue says it expects to clinically launch the product in selected sites during the third quarter of this year.