BUD DENTAL IMPLANT SYSTEM
K-Number: K902331 · 1991-07-05
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Device Summary
Frequently Asked Questions
What is the BUD DENTAL IMPLANT SYSTEM?
BUD DENTAL IMPLANT SYSTEM is a medical device that received FDA 510(k) clearance on 1991-07-05. The listed applicant is Bud Industries, Inc.. The 510(k) number is K902331.
When did BUD DENTAL IMPLANT SYSTEM receive FDA 510(k) clearance?
BUD DENTAL IMPLANT SYSTEM received FDA 510(k) clearance on 1991-07-05, under 510(k) number K902331.
Who is the listed applicant for BUD DENTAL IMPLANT SYSTEM?
The FDA 510(k) record lists Bud Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BUD DENTAL IMPLANT SYSTEM?
The FDA product code for BUD DENTAL IMPLANT SYSTEM 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 Bud Industries, 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: 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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