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Integra LifeSciences Switzerland Sàrl

US

Last updated May 24, 2026

What Integra LifeSciences Switzerland Sàrl makes

The company manufactures cerebrospinal fluid shunt systems, including ventriculo-peritoneal and atrial shunts, along with programmable shunt valves designed to regulate intracranial pressure. It also produces single-use bipolar electrosurgical handpieces and electrodes for open-surgery procedures, intracranial pressure monitors, and short-term intracerebral sensor catheters. Additional products include calibrators for intracranial pressure monitoring systems, single-use electrical connection cables, and neurosurgical procedure kits without medication.

These devices are classified under FDA regulations as Class I or Class II, with most entries listed in the FDA’s Unique Device Identifier (UDI) database. The company is based in the United States, adhering to applicable domestic regulatory standards for medical devices.

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

Information

Country
US
Address
—
LinkedIn
—
Facebook
—
Phone
+1(800)654-2873
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
480186617

Catalogue (118)

Page 3 of 3
DeviceModel / ReferenceRegistriesClassStatus
Osv Ii® 909706
FDA UDI
Class IIActive
Osv Ii® 909705
FDA UDI
Class IIActive
Licox® IP1P
FDA UDI
Class IIActive
CODMAN CERTAS® Plus 828806PL
FDA UDI
Class IIActive
Osv Ii® 909719
FDA UDI
Class IIActive
Licox® IP1
FDA UDI
Class IIActive
Codman VersaTru™ 9008150ST
FDA UDI
Class IIActive
Osv Ii® 909713
FDA UDI
Class IIActive
Osv Ii® 909701
FDA UDI
Class IIActive
DirectLink™ 826840
FDA UDI
Class IIActive
Osv Ii® 909718
FDA UDI
Class IIActive
Codman VersaTru™ 9008150SL
FDA UDI
Class IIActive
Codman® 826881
FDA UDI
Class IIActive
Codman® Certas® 828820PL
FDA UDI
Class IIActive
Integra® 990003
FDA UDI
Class IIActive
Codman® Certas® 828811PL
FDA UDI
Class IIActive
Codman® Certas® 828805PL
FDA UDI
Class IIActive
Osv Ii® 909720
FDA UDI
Class IIActive

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