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FDA 510(k)

PALTOP DENTAL IMPLANT - STERILE ACCESSORIES

K-Number: K131451 · 2013-08-22

Decision Date2013-08-22
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PALTOP DENTAL IMPLANT - STERILE ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Paltop Advanced Dental Solutions, Ltd.. It received FDA 510(k) clearance on 2013-08-22 under 510(k) number K131451. 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 PALTOP DENTAL IMPLANT - STERILE ACCESSORIES?

PALTOP DENTAL IMPLANT - STERILE ACCESSORIES is a medical device that received FDA 510(k) clearance on 2013-08-22. The listed applicant is Paltop Advanced Dental Solutions, Ltd.. The 510(k) number is K131451.

When did PALTOP DENTAL IMPLANT - STERILE ACCESSORIES receive FDA 510(k) clearance?

PALTOP DENTAL IMPLANT - STERILE ACCESSORIES received FDA 510(k) clearance on 2013-08-22, under 510(k) number K131451.

Who is the listed applicant for PALTOP DENTAL IMPLANT - STERILE ACCESSORIES?

The FDA 510(k) record lists Paltop Advanced Dental Solutions, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PALTOP DENTAL IMPLANT - STERILE ACCESSORIES?

The FDA product code for PALTOP DENTAL IMPLANT - STERILE ACCESSORIES 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.

Other records listing Paltop Advanced Dental Solutions, 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.

View all 7 devices →

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.

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.

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