# Kiltex Corp.

> Medical device manufacturer record on deviCERTS, compiled from public registries. Kiltex Corp. is a medical device manufacturer, with 9 devices listed in FDA GUDID and FDA 510(k) (FDA Class II) as of 14 Nov 2026.

- Canonical page: <https://devicerts.com/manufacturers/kiltex-corp>
- Country: United States (from the FDA registration address)
- Role: Manufacturer
- Registrations: FDA
- FDA FEI: 1527493

## Figures

- Devices: 9
- FDA recalls (matched to the firm by name): 0

## Registry facts

*Every device of the manufacturer. A device listed in two registries counts in both.*

- Registries: FDA GUDID 8, FDA 510(k) 1
- Device classes: FDA Class II 9

## Devices

The first 9 of 9, in the order of the canonical page, which lists them all.

- [Kiltex Corporation 2.0UltrasoundProbeCover(500)](https://devicerts.com/devices/kiltex-corporation-2-0ultrasoundprobeco-de2c92d4) · Class II · GUDID · status: Active
- [Kiltex Corporation 3.5UltrasoundProbeCover(720)](https://devicerts.com/devices/kiltex-corporation-3-5ultrasoundprobeco-de163901) · Class II · GUDID · status: Active
- [Kiltex Corporation 2.6UltrasoundProbeCover(100)](https://devicerts.com/devices/kiltex-corporation-2-6ultrasoundprobeco-ba620c0e) · Class II · GUDID · status: Active
- [Kiltex Corpoartion 3.5UltrasoundProbeCover(500)](https://devicerts.com/devices/kiltex-corpoartion-3-5ultrasoundprobeco) · Class II · GUDID · status: Active
- [Kiltex Corporation 2.0UltrasoundProbeCover(100)](https://devicerts.com/devices/kiltex-corporation-2-0ultrasoundprobeco) · Class II · GUDID · status: Active
- [Kiltex Corporation 2.6UltrasoundProbeCover(500)](https://devicerts.com/devices/kiltex-corporation-2-6ultrasoundprobeco) · Class II · GUDID · status: Active
- [Kiltex Corporation 3.5UltrasoundProbeCover(100)](https://devicerts.com/devices/kiltex-corporation-3-5ultrasoundprobeco-19c1894d) · Class II · GUDID · status: Active
- [Kiltex Corporation 3.5UltrasoundProbeCover(144)](https://devicerts.com/devices/kiltex-corporation-3-5ultrasoundprobeco) · Class II · GUDID · status: Active
- [Kiltex Probe Cover](https://devicerts.com/devices/kiltex-probe-cover-iyo) · ref K961029 · Class II · 510(k) · status: Active · decision 1996-07-25

## Source and citation

- Cite as: Kiltex Corp. deviCERTS medical device catalogue. https://devicerts.com/manufacturers/kiltex-corp (data as of 2026-11-14).
- Data sources: [FDA GUDID](https://accessgudid.nlm.nih.gov/), [FDA 510(k)](https://open.fda.gov/apis/device/510k/), [FDA registration and listing](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfrl/rl.cfm)
- FDA recall data as of: 2026-11-01
- Data as of: 2026-11-14
- JSON: <https://devicerts.com/manufacturers/kiltex-corp.json>
- Licence: [CC BY 4.0](https://creativecommons.org/licenses/by/4.0/). The deviCERTS layout and text are licensed under CC BY 4.0. Registry data remain under their source terms: U.S. FDA data (openFDA, AccessGUDID) are U.S. public domain; EUDAMED data are subject to the European Commission reuse terms.
- Attribution: DevicErts, https://devicerts.com/manufacturers/kiltex-corp
- Compiled by deviCERTS (devicerts.com) from public medical device registries (EUDAMED, European Commission; U.S. FDA via openFDA; AccessGUDID, U.S. National Library of Medicine). deviCERTS is not an official register and gives no regulatory advice: the record in the registry itself prevails.