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Surgrx, Inc.

United StatesFDA applicant, unverified

Devices
12

What Surgrx, Inc. makes

Surgrx, Inc. manufactures tissue sealing and vessel hemostasis devices, including the ENSEAL PTC Tissue Sealing Device, ENSEAL Vessel Sealing & Hemostasis System, and variations like the ENSEAL Powertip and ENSEAL Trio. These products are designed for laparoscopic and open surgical procedures to achieve tissue sealing and control bleeding during operations.

The company’s portfolio is regulated under FDA Class II devices, with all listed products authorised via the 510(k) pathway. These devices are intended for surgical use in the United States, where the manufacturer is based.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

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Frequently asked questions

How many devices does Surgrx, Inc. have in the registry?

The registry currently lists 12 devices for Surgrx, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Surgrx, Inc.'s devices?

Among its 12 most recently registered devices, Surgrx, Inc. has devices listed in FDA 510(k) (12 devices).

What risk classes do Surgrx, Inc.'s devices fall under?

Among its 12 most recently registered devices, the classes recorded for Surgrx, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Surgrx, Inc. in the registry?

The most recently registered devices listed for Surgrx, Inc. include ENSEAL PTC TISSUE SEALING DEVICE, ENSEAL POWERTIP, NSEAL-514D, -525D, -535D, -545D, -514RD, -525RD, -535RD, -545RD, ETRIO-314D, -325D, -335D, -345D, ENSEAL UNIVERSAL, ENSEAL TISSUE SEALING DEVICE and ENSEAL VESSEL SEALING & HEMOSTASIS SYSTEM.

Generated automatically from registry data and not verified by a human reviewer.