Categories: News

Instylla Completes Submission of Premarket Approval Application for Embrace™ Hydrogel Embolic System

BEDFORD, Mass., March 11, 2025 /PRNewswire/ — Instylla, Inc., a privately held clinical-stage company developing solutions for peripheral vascular embolotherapy, announced that it recently submitted to the U.S. Food and Drug Administration (FDA) the final module of its premarket approval application (PMA) for the Embrace Hydrogel Embolic System (HES).

In this final PMA module, Instylla has submitted clinical study results to the FDA.

In this final PMA module, Instylla has submitted clinical study results to the FDA, advancing our pursuit of the indication for the embolization of hypervascular tumors. With previous modules covering pre-clinical testing and manufacturing already completed, this marks a key step toward bringing our novel solution to the market.

“This submission marks a significant milestone for Instylla, demonstrating our team’s dedication and execution,” said Amar Sawhney, CEO of Instylla, Inc. and Managing Director of Incept, LLC. “We have leveraged the FDA’s modular submission program to streamline the approval process, enhance efficiency, and accelerate our path to market.”

About Embrace Hydrogel Embolic System:

Embrace HES is an investigational device intended to embolize hypervascular tumors in vessels ≤ 5 mm. Embrace HES consists of two injectable liquid precursors that solidify when simultaneously delivered into blood vessels, forming a soft hydrogel that fills the vessel lumens during embolization. Embrace HES embolization uses no solvents, does not need sizing to the vessel diameter, and eliminates the possibility of catheter entrapment. Its main components are water and polyethylene glycol (PEG).

About Instylla:

Instylla, Inc. is a privately held company based in Bedford, MA, focused on developing novel resorbable embolic agents to advance interventional radiology, with initial clinical applications in interventional oncology and the peripheral vasculature. Instylla was founded in 2017 by Incept LLC and is funded by several leading venture capital groups.  

To learn more, please visit https://www.instylla.com/

Caution: Investigational Device. Limited by Federal (or US) law to investigational use only. Not available for sale.

View original content to download multimedia:https://www.prnewswire.com/news-releases/instylla-completes-submission-of-premarket-approval-application-for-embrace-hydrogel-embolic-system-302397602.html

SOURCE Instylla, Inc.

Staff

Recent Posts

AI-Era Position Statement to Protect the Integrity of Healthcare, Technology, and Services Benchmarking published by Black Book Research

Black Book outlines an AI-era integrity architecture for healthcare benchmarking, instrumentation hardening, tiered verification, real-time…

21 hours ago

New employee representative on the Board of Directors of Novo Nordisk A/S

Bagsværd, Denmark, 31 January 2026 – Thomas Rantzau, employee representative on the Board of Directors since…

21 hours ago

Embers to Empowerment: The Womb Room Reopens in Govans, Expanding Community-Centered Perinatal Care After Hampden Fire

Baltimore, Maryland, Jan. 31, 2026 (GLOBE NEWSWIRE) -- After sustaining water damage during the massive…

21 hours ago

Oxford Healthspan to Introduce New Primeadine® GF Powder Through a ‘Longevity Shot’ Experience During Grammy Week in Los Angeles

Science-Backed Spermidine Ritual Brings Cellular Renewal to a High-Performance Cultural Moment Primeadine Longevity Shot Primeadine…

21 hours ago

Enzon Announces Commencement of Exchange Offer Relating to Series C Non-Convertible Redeemable Preferred Stock in Connection With Viskase Merger

CRANFORD, N.J., Jan. 30, 2026 (GLOBE NEWSWIRE) -- Enzon Pharmaceuticals, Inc. (OTCQB: ENZN) (“Enzon” or…

21 hours ago

Park Dental Partners Announces Dates for Fourth Quarter and Full Year 2025 Earnings Release and Conference Call

MINNEAPOLIS, Jan. 30, 2026 (GLOBE NEWSWIRE) -- Park Dental Partners, Inc. (NASDAQ: PARK), a leading…

21 hours ago