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Integra Pain Management

Last updated September 17, 2026

Information

Country: US
Address: 3498 WEST 2400 SOUTH, West Valley City, UT, 84119
Website: —
LinkedIn: —
Facebook: —
Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 1000138491
DUNS Number: —

Catalogue (819)

Page 10 of 17

Device	Model / Reference	Registries	Class	Status
Integra®	3405062	FDA UDI	Class II	Unknown
Integra®	ITRW2035	FDA UDI	N/A	Unknown
Integra®	CUS702	FDA UDI	N/A	Unknown
Integra®	CUS1207-01	FDA UDI	N/A	Unknown
Integra®	3404697	FDA UDI	N/A	Unknown
Integra®	PITRW1735	FDA UDI	N/A	Unknown
Integra®	CUS1072-01	FDA UDI	N/A	Unknown
Integra®	CUS161	FDA UDI	Class II	Unknown
Integra®	CUS1428	FDA UDI	Class II	Unknown
Integra®	31254	FDA UDI	N/A	Active
Integra®	INS7040	FDA UDI	N/A	Active
Integra®	3404388	FDA UDI	Class II	Unknown
Integra®	3404920	FDA UDI	N/A	Unknown
Integra®	3404652	FDA UDI	N/A	Unknown
Integra®	3405179	FDA UDI	N/A	Unknown
Integra®	3404816	FDA UDI	Class II	Unknown
Integra®	3405221	FDA UDI	N/A	Unknown
Integra®	3405193	FDA UDI	N/A	Unknown
Integra®	CUS1368	FDA UDI	N/A	Unknown
Integra®	CUS1352-02	FDA UDI	N/A	Unknown
Integra®	3404791	FDA UDI	Class II	Unknown
Integra®	20-2160	FDA UDI	N/A	Unknown
Integra®	3405226	FDA UDI	Class II	Unknown
Integra®	INSHITHND	FDA UDI	N/A	Active
Integra®	CUS1664-01	FDA UDI	N/A	Unknown
Integra®	3104020	FDA UDI	Class II	Unknown
Integra®	CUS1207-01	FDA UDI	Class II	Unknown
Integra®	3403134	FDA UDI	N/A	Unknown
Integra®	CUS1662	FDA UDI	N/A	Unknown
Integra®	INSHITH	FDA UDI	N/A	Active
Integra®	3404951	FDA UDI	N/A	Unknown
Owl®	RF22-100-10CS	FDA UDI	N/A	Unknown
Integra®	SP0088	FDA UDI	Class II	Active
Owl®	RF22-100-5	FDA UDI	N/A	Unknown
Integra®	CUS1192-03	FDA UDI	N/A	Unknown
Integra®	SS1867	FDA UDI	N/A	Unknown
Integra®	3805428	FDA UDI	Class II	Unknown
Integra®	13-2890	FDA UDI	N/A	Unknown
Integra®	CUS1600	FDA UDI	Class II	Unknown
Integra®	CUS1346-01	FDA UDI	N/A	Unknown
Integra®	3405111	FDA UDI	N/A	Unknown
Integra®	3405157	FDA UDI	Class II	Unknown
Integra®	3404544	FDA UDI	N/A	Unknown
Integra®	10-2558	FDA UDI	N/A	Unknown
Integra®	SS2252	FDA UDI	Class II	Unknown
Integra®	CUS1517	FDA UDI	N/A	Unknown
Accu-Disc™	5050	FDA UDI	N/A	Unknown
Integra®	3403904-3	FDA UDI	N/A	Unknown
Integra®	12-2893	FDA UDI	N/A	Unknown
Integra®	3404799	FDA UDI	N/A	Unknown

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Authorities

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FDA Recalls (2)

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.