S.E.A.L. Hemostatic Wound Spray (K210751) - FDA 510(k) Clearance

K210751 is an FDA 510(k) clearance for the S.E.A.L. Hemostatic Wound Spray. Classified as Hemostatic Wound Dressing Without Thrombin Or Other Biologics (product code QSY).

Submitted by Bc3 Technologies, Inc. (Baltimore, US). The FDA issued a Cleared decision on February 2, 2023 after a review of 692 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the General & Plastic Surgery FDA review panel. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: High-complexity regulatory submission. Elevated predicate reliance profile. The extended review timeline suggests the FDA required additional documentation before confirming substantial equivalence - a pattern common in complex or first-of-kind General & Plastic Surgery submissions.

View all Bc3 Technologies, Inc. devices