DENTINSENSE B/C
K-Number: K965138 · 1997-02-14
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Device Summary
Frequently Asked Questions
What is the DENTINSENSE B/C?
DENTINSENSE B/C is a medical device that received FDA 510(k) clearance on 1997-02-14. The listed applicant is Centrix, Inc.. The 510(k) number is K965138.
When did DENTINSENSE B/C receive FDA 510(k) clearance?
DENTINSENSE B/C received FDA 510(k) clearance on 1997-02-14, under 510(k) number K965138.
Who is the listed applicant for DENTINSENSE B/C?
The FDA 510(k) record lists Centrix, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DENTINSENSE B/C?
The FDA product code for DENTINSENSE B/C is KLE.
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 Centrix, Inc. 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.
Related Devices (Code: KLE)
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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