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Integra Pain Management

Last updated September 17, 2026

Information

Page 17 of 17

Device	Model / Reference	Registries	Class	Status
Integra®	SP0087	FDA UDI	Class II	Active
Integra®	HITHTA04	FDA UDI	N/A	Unknown
Integra®	SP0075	FDA UDI	Class II	Active
Integra®	3405036	FDA UDI	N/A	Unknown
Integra®	3405059	FDA UDI	N/A	Unknown
Integra®	3404625	FDA UDI	N/A	Unknown
Integra®	3402996	FDA UDI	N/A	Unknown
Integra®	CUS701-01	FDA UDI	N/A	Unknown
Integra®	3405060	FDA UDI	Class II	Unknown
Integra®	20-1462-01	FDA UDI	N/A	Unknown
Integra®	3404388	FDA UDI	N/A	Unknown
Integra®	SS3157	FDA UDI	N/A	Unknown
Integra®	3404814	FDA UDI	N/A	Unknown
Integra®	3405186	FDA UDI	Class II	Unknown
Integra®	CUS1021	FDA UDI	N/A	Unknown
Integra®	3405191	FDA UDI	N/A	Unknown
Integra®	CUS1119-01	FDA UDI	N/A	Unknown
Integra®	3303277	FDA UDI	N/A	Unknown
Integra®	10-1879-00	FDA UDI	N/A	Unknown

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Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Date	Recall No.	Class	Status	Reason
Jul 7, 2008	Z-2335-2008	—	terminated	Radiation reduction gloves were labeled as "Latex-free", but contain natural rubber latex.
Mar 18, 2008	Z-1635-2008	—	terminated	Hep-Lock Flush vials included in Integra's PICC Insertion Trays contain a heparin component that has been recalled by Baxter for contaminated heparin.