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Tenaxis Medical, Inc.

US

Last updated May 30, 2026

What Tenaxis Medical, Inc. makes

Tenaxis Medical, Inc. manufactures surgical sealants and adhesive tips derived from animal sources, designed to prevent leakage during internal procedures. Their portfolio includes a liquid sealant and disposable application tips used in surgical settings to reinforce tissue integrity.

The company’s products are classified as Class III medical devices under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What does Tenaxis Medical, Inc. manufacture?

Tenaxis Medical, Inc. produces surgical sealants and adhesive tips derived from animal sources, designed to prevent leakage during internal surgical procedures. Their portfolio includes a liquid sealant and disposable application tips used to reinforce tissue integrity in surgical settings.

Where is Tenaxis Medical, Inc. based?

Tenaxis Medical, Inc. is based in the United States. The company operates from its headquarters located within the country, where it develops and manufactures its medical devices.

Which regulatory registries list Tenaxis Medical's devices?

Tenaxis Medical's devices are listed in the FDA's Unique Device Identifier (UDI) database. This registry tracks medical devices through unique identifiers to ensure proper identification and tracking throughout their lifecycle.

How are Tenaxis Medical's devices classified?

Tenaxis Medical's devices are classified as Class III medical devices under FDA regulations. This is the highest risk classification, indicating that the devices require the most stringent regulatory controls due to their potential risk to patient safety.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
Website
xxx.xxx
LinkedIn
—
Facebook
—
Phone
650-691-9016
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
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DUNS Number
783546109

Catalogue (5)

DeviceModel / ReferenceRegistriesClassStatus
PreveLeak™ 10 pack Tips 10 pack Tips
FDA UDI
Class IIIActive
PreveLeak™ Surgical Sealant 2.5 ml
FDA UDI
Class IIIActive
PreveLeak™ Surgical Sealant 4 ml
FDA UDI
Class IIIActive
PreveLeak™ Surgical Sealant 2.5 ml
FDA UDI
Class IIIActive
PreveLeak™ Surgical Sealant 5 ml
FDA UDI
Class IIIActive

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