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FDA 510(k)

LINGLOCK

K-Number: K061042 · 2007-01-19

ApplicantSybron Dental Specialties
Decision Date2007-01-19
Product CodeDYW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LINGLOCK is the device name listed in this FDA 510(k) record. The listed applicant is Sybron Dental Specialties. It received FDA 510(k) clearance on 2007-01-19 under 510(k) number K061042. The device is classified under product code DYW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LINGLOCK?

LINGLOCK is a medical device that received FDA 510(k) clearance on 2007-01-19. The listed applicant is Sybron Dental Specialties. The 510(k) number is K061042.

When did LINGLOCK receive FDA 510(k) clearance?

LINGLOCK received FDA 510(k) clearance on 2007-01-19, under 510(k) number K061042.

Who is the listed applicant for LINGLOCK?

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

What is the FDA product code for LINGLOCK?

The FDA product code for LINGLOCK is DYW.

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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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