FDA Device Intelligence
Home › Pramand LLC › SpineSeal Spine Sealant

SpineSeal Spine Sealant

Pramand LLC · Model SS-2055 · UDI-DI 00860010683729

NQR Prescription
0
510(k) clearances
576
Adverse events (2 deaths)
0
Recalls
15
Facilities

Description

The SpineSeal Spine Sealant is indicated as an adjuct to sutured dural repair during spine surgery to provide a watertight closure.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.