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FDA 510(k)

A.B. DENTAL DEVICES

K-Number: K051719 · 2006-03-21

ApplicantA.B. Dental Devices , Ltd.
Decision Date2006-03-21
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

A.B. DENTAL DEVICES is the device name listed in this FDA 510(k) record. The listed applicant is A.B. Dental Devices , Ltd.. It received FDA 510(k) clearance on 2006-03-21 under 510(k) number K051719. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the A.B. DENTAL DEVICES?

A.B. DENTAL DEVICES is a medical device that received FDA 510(k) clearance on 2006-03-21. The listed applicant is A.B. Dental Devices , Ltd.. The 510(k) number is K051719.

When did A.B. DENTAL DEVICES receive FDA 510(k) clearance?

A.B. DENTAL DEVICES received FDA 510(k) clearance on 2006-03-21, under 510(k) number K051719.

Who is the listed applicant for A.B. DENTAL DEVICES?

The FDA 510(k) record lists A.B. Dental Devices , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for A.B. DENTAL DEVICES?

The FDA product code for A.B. DENTAL DEVICES is DZE.

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 A.B. Dental Devices , Ltd. 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.

K250806Dental Implant SystemK112440AB DENTAL DEVICES IMPLANTS AND ACCESSORIES

Related Devices (Code: DZE)

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.

K261392TriActive Dental Implant SystemParagon Implant Mfg., LLCK260463ZEROS Dental Implant SystemZeros Co., Ltd.K251188UNIQA® Dental Implants SystemUniqa Dental, Ltd.K251232MegaGen Zygoma Dental Implant SystemMegagen Implant Co., Ltd.K250806Dental Implant SystemA.B. Dental Devices , Ltd.K260006INOSS SystemInosys, 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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