SOLIDEX
K-Number: K972292 · 1997-10-29
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Device Summary
Frequently Asked Questions
What is the SOLIDEX?
SOLIDEX is a medical device that received FDA 510(k) clearance on 1997-10-29. The listed applicant is Shofu Dental Corp.. The 510(k) number is K972292.
When did SOLIDEX receive FDA 510(k) clearance?
SOLIDEX received FDA 510(k) clearance on 1997-10-29, under 510(k) number K972292.
Who is the listed applicant for SOLIDEX?
The FDA 510(k) record lists Shofu Dental Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SOLIDEX?
The FDA product code for SOLIDEX is EBF.
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 Shofu Dental Corp. 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: EBF)
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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