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XODUS MEDICAL, INC.

United States·US-MF-000003939

Last updated September 17, 2026

What XODUS MEDICAL, INC. makes

Xodus Medical, Inc. manufactures single-use procedural medication labeling sets, operating table patient positioning sets, freestanding patient positioners, monopolar electrosurgical electrodes for open surgery, sharp surgical instrument counting trays or pads, skin marking pens, operating room turnover kits, and reusable operating table patient pressure distribution pads.

The company's devices are classified as Class I and Class II medical devices and are listed in the FDA's Unique Device Identification (fda_udi) registry. Xodus Medical, Inc. 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 types of medical devices does Xodus Medical, Inc. manufacture?

Xodus Medical, Inc. manufactures procedural medication labeling sets, operating table patient positioning sets, freestanding patient positioners, monopolar electrosurgical electrodes for open surgery, sharp surgical instrument counting trays or pads, skin marking pens, operating room turnover kits, and reusable operating table patient pressure distribution pads. These products are designed for single-use or reusable applications in surgical and procedural settings, as specified in the device data.

Where is Xodus Medical, Inc. based?

Xodus Medical, Inc. is based in the United States, as explicitly stated in the device data under the COUNTRY field and confirmed in the SUMMARY section, which notes the company's location without referencing any specific city, state, or facility details beyond the country level.

In which regulatory registry are Xodus Medical, Inc.'s devices listed?

Xodus Medical, Inc.'s devices are listed in the FDA's Unique Device Identification (fda_udi) registry, as indicated in the LISTED IN field and reiterated in the SUMMARY, which confirms the company's devices are included in this specific U.S. regulatory system for device tracking and identification.

How are Xodus Medical, Inc.'s devices classified under regulatory frameworks?

Xodus Medical, Inc.'s devices are classified as Class I and Class II medical devices, according to the DEVICE CLASSES field in the provided data. This classification reflects the risk-based regulatory categorization used by the FDA, where Class I devices are low-risk and Class II devices require special controls, but neither classification implies approval or clearance of the company itself.

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

Information

Country
United States
Address
702, Prominence Drive, New Kensington, United States
LinkedIn
—
Facebook
—
Phone
7243375500
PRRC Contact
Paul Lloyd
EUDAMED SRN
US-MF-000003939
FDA FEI Number
1000221205
DUNS Number
868042664

Catalogue (3442)

Page 3 of 69
DeviceModel / ReferenceRegistriesClassStatus
NSCL21941 Custom Med Label Pack NSCL21941
FDA UDI
Class IActive
NSCL20672 Custom Med Label Pack NSCL20672
FDA UDI
Class IActive
CL21400 Custom Med Label Pack CL21400
FDA UDI
Class IActive
CL23908 Custom Med Label Pack CL23908
FDA UDI
Class IActive
SPK10673 Jackson Table Kit SPK10673
FDA UDI
Class IActive
NSCL23194 Custom Med Label Pack NSCL23194
FDA UDI
Class IActive
SPK10495 Jackson Kit SPK10495
FDA UDI
Class IActive
NSCL24778 Custom Med Label Pack NSCL24778
FDA UDI
Class IActive
NSCL21265 Custom Med Label Pack NSCL21265
FDA UDI
Class IActive
CL20649 Custom Med Label Pack CL20649
FDA UDI
Class IActive
41861 Reusable Gel Pediatric Chest Roll 12" x 3" x 3" 41861
FDA UDI
Class IActive
NSCL22106 Custom Med Label Pack NSCL22106
FDA UDI
Class IActive
RTK10162 Room Turnover Kit RTK10162
FDA UDI
Class IActive
80522 The Camel Mat - 8mm Absorbent Mat, Non-Slip; 32"x40", Yellow 80522
FDA UDI
Class IActive
NSCL24802 Custom Med Label Pack NSCL24802
FDA UDI
Class IActive
NSCL23317 Custom Med Label Pack NSCL23317
FDA UDI
Class IActive
SPK10181 Surgical BackPack Kit SPK10181
FDA UDI
Class IActive
NSCL20380 Custom Med Label Pack NSCL20380
FDA UDI
Class IActive
NSCL22053 Custom Med Label Pack NSCL22053
FDA UDI
Class IActive
SPK10372 Wilson Frame Kit SPK10372
FDA UDI
Class IActive
CL20495 Custom Med Label Pack CL20495
FDA UDI
Class IActive
CL25263 Custom Med Label Pack CL25263
FDA UDI
Class IActive
5CM Tungsten Needle Ext Ins; No Coating; Blue Ins; Black Ext Ins NS20102
FDA UDI
Class IIActive
NSCL22751 Custom Med Label Pack NSCL22751
FDA UDI
Class IActive
CL22001 Custom Med Label Pack CL22001
FDA UDI
Class IActive
NSCL20937 Custom Med Label Pack NSCL20937
FDA UDI
Class IActive
NSCL21368 Custom Med Label Pack NSCL21368
FDA UDI
Class IActive
NSCL20745 Custom Med Label Pack NSCL20745
FDA UDI
Class IActive
CL21608 Custom Med Label Pack CL21608
FDA UDI
Class IActive
CL21954 Custom Med Label Pack CL21954
FDA UDI
Class IActive
NSCL24305 Custom Med Label Pack NSCL24305
FDA UDI
Class IActive
NSCL22272 Custom Med Label Pack NSCL22272
FDA UDI
Class IActive
NSCL21953 Custom Med Label Pack NSCL21953
FDA UDI
Class IActive
6.5" Blade Tip Ext Insulation; Blue PTFE; Blue Ins; Black Ext Ins; PL 20015SPI
FDA UDI
Class IIActive
SPK11074 Jackson Kit SPK11074
FDA UDI
Class IActive
NSCL22924 Custom Med Label Pack NSCL22924
FDA UDI
Class IActive
30978 See Sharp - Enhanced Intraoperative Laparoscope Cleaning & Defogging 30978
FDA UDI
Class IIActive
NSCL22567 Custom Med Label Pack NSCL22567
FDA UDI
Class IActive
NSCL24356 Custom Med Label Pack NSCL24356
FDA UDI
Class IActive
CL23968 Custom Med Label Pack CL23968
FDA UDI
Class IActive
SPK10443 Jackson Table Kit SPK10443
FDA UDI
Class IActive
CL22693 Custom Med Label Pack CL22693
FDA UDI
Class IActive
NSCL22976 Custom Med Label Pack NSCL22976
FDA UDI
Class IActive
41813 Reusable Gel Small Armboard 41813
FDA UDI
Class IActive
40442 Child Head Rest 9'' 40442
FDA UDI
Class IActive
NSCL22275 Custom Med Label Pack NSCL22275
FDA UDI
Class IActive
CL21649 Custom Med Label Pack CL21649
FDA UDI
Class IActive
NSCL20498 Custom Med Label Pack NSCL20498
FDA UDI
Class IActive
CL24078 Custom Med Label Pack CL24078
FDA UDI
Class IActive
40466 Ocular Head Rest w/Cover 40466
FDA UDI
Class IActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

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.

The FDA recall records for Xodus Medical, Inc. show 3 recall records. The earliest and most recent recall records were both initiated on 2019-09-19. All recalls have a status of terminated. The reasons given for the recalls include that the sterile barrier of some devices may have been affected.

AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.

DateRecall No.ClassStatusReason
Sep 19, 2019Z-0150-2020—terminated

The sterile barrier of some devices may have been affected

Sep 19, 2019Z-0151-2020—terminated

The sterile barrier of some devices may have been affected

Sep 19, 2019Z-0149-2020—terminated

The sterile barrier of some devices may have been affected