ENDOSSOUS IMPLANTS
K-Number: K021322 · 2002-07-24
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Device Summary
Frequently Asked Questions
What is the ENDOSSOUS IMPLANTS?
ENDOSSOUS IMPLANTS is a medical device that received FDA 510(k) clearance on 2002-07-24. The listed applicant is Intra-Lock International. The 510(k) number is K021322.
When did ENDOSSOUS IMPLANTS receive FDA 510(k) clearance?
ENDOSSOUS IMPLANTS received FDA 510(k) clearance on 2002-07-24, under 510(k) number K021322.
Who is the listed applicant for ENDOSSOUS IMPLANTS?
The FDA 510(k) record lists Intra-Lock International as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ENDOSSOUS IMPLANTS?
The FDA product code for ENDOSSOUS IMPLANTS is DZE.
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 Intra-Lock International 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: DZE)
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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