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FDA 510(k)

JET BLUE BITE

K-Number: K051243 · 2005-06-23

Decision Date2005-06-23
Product CodeELW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

JET BLUE BITE is the device name listed in this FDA 510(k) record. The listed applicant is Coltene/Whaledent AG. It received FDA 510(k) clearance on 2005-06-23 under 510(k) number K051243. The device is classified under product code ELW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JET BLUE BITE?

JET BLUE BITE is a medical device that received FDA 510(k) clearance on 2005-06-23. The listed applicant is Coltene/Whaledent AG. The 510(k) number is K051243.

When did JET BLUE BITE receive FDA 510(k) clearance?

JET BLUE BITE received FDA 510(k) clearance on 2005-06-23, under 510(k) number K051243.

Who is the listed applicant for JET BLUE BITE?

The FDA 510(k) record lists Coltene/Whaledent AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for JET BLUE BITE?

The FDA product code for JET BLUE BITE is ELW.

Other records listing Coltene/Whaledent AG 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 14 devices →

Related Devices (Code: ELW)

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

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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