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FDA 510(k)

WDS X-POD AND ZEN-X DIGITAL X-RAY SENSORS

K-Number: K100960 · 2010-10-21

ApplicantCefla Dental Group
Decision Date2010-10-21
Product CodeMUH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

WDS X-POD AND ZEN-X DIGITAL X-RAY SENSORS is the device name listed in this FDA 510(k) record. The listed applicant is Cefla Dental Group. It received FDA 510(k) clearance on 2010-10-21 under 510(k) number K100960. The device is classified under product code MUH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WDS X-POD AND ZEN-X DIGITAL X-RAY SENSORS?

WDS X-POD AND ZEN-X DIGITAL X-RAY SENSORS is a medical device that received FDA 510(k) clearance on 2010-10-21. The listed applicant is Cefla Dental Group. The 510(k) number is K100960.

When did WDS X-POD AND ZEN-X DIGITAL X-RAY SENSORS receive FDA 510(k) clearance?

WDS X-POD AND ZEN-X DIGITAL X-RAY SENSORS received FDA 510(k) clearance on 2010-10-21, under 510(k) number K100960.

Who is the listed applicant for WDS X-POD AND ZEN-X DIGITAL X-RAY SENSORS?

The FDA 510(k) record lists Cefla Dental Group as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WDS X-POD AND ZEN-X DIGITAL X-RAY SENSORS?

The FDA product code for WDS X-POD AND ZEN-X DIGITAL X-RAY SENSORS is MUH.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing Cefla Dental Group as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K101661MYRAY HYPERION

Related Devices (Code: MUH)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K251793SOTA Cloud Smart Sensor (1.5)Sota Cloud Corp.K252570EzSensor HD, EzSensor UHDQpix Solutions, Inc.K250687Cocoon Solo (DX-7020s)Dexcowin Global, Inc.K251206Digital X-Ray DentiMax Pro Imaging SystemDentimax, Inc.K240040VistaPano S Ceph 2.0 (VistaPano S Ceph); VistaPano S 2.0 (VistaPano S); ProVecta S-Pan Ceph 2.0 (ProVecta S-Pan Ceph); ProVecta S-Pan 2.0 (ProVecta S-Pan)VATECH Co., Ltd.K242778X Sensor (Model: IOS-A15IF, HDI-15DGF)Qpix Solutions, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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