WEDGES, RETAINING, MATRIX
K-Number: K772314 · 1978-01-03
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Device Summary
Frequently Asked Questions
What is the WEDGES, RETAINING, MATRIX?
WEDGES, RETAINING, MATRIX is a medical device that received FDA 510(k) clearance on 1978-01-03. The listed applicant is Den-Mat Corp.. The 510(k) number is K772314.
When did WEDGES, RETAINING, MATRIX receive FDA 510(k) clearance?
WEDGES, RETAINING, MATRIX received FDA 510(k) clearance on 1978-01-03, under 510(k) number K772314.
Who is the listed applicant for WEDGES, RETAINING, MATRIX?
The FDA 510(k) record lists Den-Mat Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for WEDGES, RETAINING, MATRIX?
The FDA product code for WEDGES, RETAINING, MATRIX is DZN.
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 Den-Mat 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: DZN)
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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