FDA 510(k)

Apex Dental Sensors

K-Number: K163282 · 2017-02-28

Decision Date2017-02-28

Product CodeMUH

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

Apex Dental Sensors is the device name listed in this FDA 510(k) record. The listed applicant is Masterlink, LLC. It received FDA 510(k) clearance on 2017-02-28 under 510(k) number K163282. 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 Apex Dental Sensors?

Apex Dental Sensors is a medical device that received FDA 510(k) clearance on 2017-02-28. The listed applicant is Masterlink, LLC. The 510(k) number is K163282.

When did Apex Dental Sensors receive FDA 510(k) clearance?

Apex Dental Sensors received FDA 510(k) clearance on 2017-02-28, under 510(k) number K163282.

Who is the listed applicant for Apex Dental Sensors?

The FDA 510(k) record lists Masterlink, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Apex Dental Sensors?

The FDA product code for Apex Dental Sensors is MUH.

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

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