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XODUS MEDICAL, INC.

United States·US-MF-000003939

Last updated September 17, 2026

Information

Country: United States
Address: 702, Prominence Drive, New Kensington, United States
Website: www.xodusmedical.com
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: 7243375500
PRRC Contact: Paul Lloyd
EUDAMED SRN: US-MF-000003939
FDA FEI Number: 1000221205
DUNS Number: 868042664

Catalogue (3442)

Page 1 of 69

Device	Model / Reference	Registries	Class	Status
CL22960 Custom Med Label Pack	CL22960	FDA UDI	Class I	Active
CL24796 Custom Med Label Pack	CL24796	FDA UDI	Class I	Active
CL21928 Custom Med Label Pack	CL21928	FDA UDI	Class I	Active
NSCL23312 Custom Med Label Pack	NSCL23312	FDA UDI	Class I	Active
NS10675 Safety Foam	NS10675	FDA UDI	Class I	Active
NSCL22544 Custom Med Label Pack	NSCL22544	FDA UDI	Class I	Active
40945 Intra-Leg Lateral Positioner 3''	40945	FDA UDI	Class I	Active
CL21953 Custom Med Label Pack	CL21953	FDA UDI	Class I	Active
CL24220 Custom Med Label Pack	CL24220	FDA UDI	Class I	Active
NSCL24789 Custom Med Label Pack	NSCL24789	FDA UDI	Class I	Active
NSCL21810 Custom Med Label Pack	NSCL21810	FDA UDI	Class I	Active
CL22854 Custom Med Label Pack	CL22854	FDA UDI	Class I	Active
CL22267 Custom Med Label Pack	CL22267	FDA UDI	Class I	Active
CL21604 Custom Med Label Pack	CL21604	FDA UDI	Class I	Active
NS70464TYVEK Needle Counter Blade Remover Tyvek Pouch Non Sterile	NS70464TYVEK	FDA UDI	Class I	Active
NSCL20427 Custom Med Label Pack	NSCL20427	FDA UDI	Class I	Active
NSCL20335 Custom Med Label Pack	NSCL20335	FDA UDI	Class I	Active
NSCL20381 Custom Med Label Pack	NSCL20381	FDA UDI	Class I	Active
CL21293 Custom Med Label Pack	CL21293	FDA UDI	Class I	Active
33cm Laparoscopic Narrow Curved Blade; Blue PTFE; Black Insulation	20155ACT	FDA UDI	Class II	Active
NSCL20747 Custom Med Label Pack	NSCL20747	FDA UDI	Class I	Active
CL21363 Custom Med Label Pack	CL21363	FDA UDI	Class I	Active
80855 Reusable Magnetic Transfer Zone 12" x 8"	80855	FDA UDI	Class I	Active
Yankauer Suction Tip - Straight / Vented	10877	FDA UDI	Class II	Active
SPK10470 Jackson Kit	SPK10470	FDA UDI	Class I	Active
NSCL22147 Custom Med Label Pack	NSCL22147	FDA UDI	Class I	Active
CL21567 Custom Med Label Pack	CL21567	FDA UDI	Class I	Active
NSCL20732 Custom Med Label Pack	NSCL20732	FDA UDI	Class I	Active
CL21087 Custom Med Label Pack	CL21087	FDA UDI	Class I	Active
NSCL24518 Custom Med Label Pack	NSCL24518	FDA UDI	Class I	Active
CL21103 Custom Med Label Pack	CL21103	FDA UDI	Class I	Active
SPK10184 Orthopedic Fracture Kit	SPK10184	FDA UDI	Class I	Active
40763 Beach Chair Head Restraint	40763	FDA UDI	Class I	Active
SPK10596 Jackson Table Kit	SPK10596	FDA UDI	Class I	Active
NSCL22350 Custom Med Label Pack	NSCL22350	FDA UDI	Class I	Active
CL21767 Custom Med Label Pack	CL21767	FDA UDI	Class I	Active
NS10405 Permanent Marker; Round Pen Regular Tip (purple)	NS10405	FDA UDI	Class I	Active
90111 Safety Cartridge #11 Carbon Steel Blade Orange Cartridge	90111	FDA UDI	Class I	Active
SPK10799 Jackson Table Kit	SPK10799	FDA UDI	Class I	Active
NSCL24306 Custom Med Label Pack	NSCL24306	FDA UDI	Class I	Active
CL22263 Custom Med Label Pack	CL22263	FDA UDI	Class I	Active
70211ROI Magnet/Foam Strips 30-60 Count. PL	70211ROI	FDA UDI	Class I	Active
CL21770 Custom Med Label Pack	CL21770	FDA UDI	Class I	Active
NSCL21078 Custom Med Label Pack	NSCL21078	FDA UDI	Class I	Active
Yankauer Suction Tip 10 Degree Angle - Straight Tip / Non-Vented	10886	FDA UDI	Class II	Active
NSCL23058 Custom Med Label Pack	NSCL23058	FDA UDI	Class I	Active
NSCL22547 Custom Med Label Pack	NSCL22547	FDA UDI	Class I	Active
NSCL24353 Custom Med Label Pack	NSCL24353	FDA UDI	Class I	Active
NSCL21274 Custom Med Label Pack	NSCL21274	FDA UDI	Class I	Active
RTK10203 Room Turnover Kit	RTK10203	FDA UDI	Class I	Active

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Authorised Representatives

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Importers

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Notified Bodies

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Authorities

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FDA Recalls (3)

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
Sep 19, 2019	Z-0150-2020	—	terminated	The sterile barrier of some devices may have been affected
Sep 19, 2019	Z-0151-2020	—	terminated	The sterile barrier of some devices may have been affected
Sep 19, 2019	Z-0149-2020	—	terminated	The sterile barrier of some devices may have been affected