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FDA 510(k)

IMPLANTMASTER

K-Number: K042212 · 2004-10-21

ApplicantI-Dent
Decision Date2004-10-21
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

IMPLANTMASTER is the device name listed in this FDA 510(k) record. The listed applicant is I-Dent. It received FDA 510(k) clearance on 2004-10-21 under 510(k) number K042212. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMPLANTMASTER?

IMPLANTMASTER is a medical device that received FDA 510(k) clearance on 2004-10-21. The listed applicant is I-Dent. The 510(k) number is K042212.

When did IMPLANTMASTER receive FDA 510(k) clearance?

IMPLANTMASTER received FDA 510(k) clearance on 2004-10-21, under 510(k) number K042212.

Who is the listed applicant for IMPLANTMASTER?

The FDA 510(k) record lists I-Dent as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IMPLANTMASTER?

The FDA product code for IMPLANTMASTER is LLZ.

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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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