Data / Medical devices / United States / Xenex Disinfection Services Inc.
Xenex Disinfection Services Inc.: FDA-registered device maker in San Antonio, TX, United States, 1 510(k) clearance
Xenex Disinfection Services Inc. is registered with the FDA (registration 3014531752) in San Antonio, TX, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated September 1, 2023. 1 recall event names it as the recalling firm. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3014531752
- Address
- 1074 Arion Circle Suite 116, San Antonio, TX, United States, 78216
- Owner or operator
- Xenex Disinfection Services Inc. (10086819)
- Roles
- Complaint file establishment, Manufacturer, Remanufacturer
- First device listed
- December 14, 2022
- Registered through
- 2026
- Brand names listed
- LightStrike (LSMUV6-FT), LightStrike (LSMUV6-SL), LightStrike (PXUV4D), LightStrike (PXUV5D), LightStrike+ (MXSUV1-FT), LightStrike+ (MXSUV1-SL)
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Antimicrobial Keyboard | OSZ | 2 | Complaint file establishment | accessdata.fda.gov |
| Whole Room Microbial Reduction Device | QXJ | 2 | Complaint file establishment, Manufacturer, Remanufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| September 1, 2023 | DEN230007 | LightStrike+ (MXSUV1-SL and MXSUV1-FT) | QXJ | Unknown | Xenex Disinfection Services, Inc. | accessdata.fda.gov |
Recalls
Recall events where this establishment is the recalling firm, matched on its FEI.
| Initiated | Event | Class | Status | Product | Reason | Source |
|---|---|---|---|---|---|---|
| March 18, 2024 | 94258 | Class II | Ongoing | LightStrike Blackout Curtains, Part numbers; 610-00008, 610-00009, 610-00019, 610-00020, and 610-00024, used with the LightStrike Germ-Zapping Robots Models: PXUV4D, PXUV5D, LSMUV6-FT, or LSMUV6-SL, for whole room microb | Blackout curtains are no longer recommended as a protective barrier against UV/Ozone exposure to a bystander standing in the same room, but on the other side of the curtain from where a microbial reduction device UV cycle is taking place. Bystanders in the room during the cycle may experience temporary skin reddening, feeling of sand in eyes, nausea, headach | accessdata.fda.gov |
Updated April 23, 2024. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.