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FDA 510(k)

ACE CYLINDER DENTAL IMPLANT

K-Number: K954605 · 1996-06-05

Decision Date1996-06-05
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ACE CYLINDER DENTAL IMPLANT is the device name listed in this FDA 510(k) record. The listed applicant is Ace Surgical Supply Co., Inc.. It received FDA 510(k) clearance on 1996-06-05 under 510(k) number K954605. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACE CYLINDER DENTAL IMPLANT?

ACE CYLINDER DENTAL IMPLANT is a medical device that received FDA 510(k) clearance on 1996-06-05. The listed applicant is Ace Surgical Supply Co., Inc.. The 510(k) number is K954605.

When did ACE CYLINDER DENTAL IMPLANT receive FDA 510(k) clearance?

ACE CYLINDER DENTAL IMPLANT received FDA 510(k) clearance on 1996-06-05, under 510(k) number K954605.

Who is the listed applicant for ACE CYLINDER DENTAL IMPLANT?

The FDA 510(k) record lists Ace Surgical Supply Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACE CYLINDER DENTAL IMPLANT?

The FDA product code for ACE CYLINDER DENTAL IMPLANT 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 Ace Surgical Supply Co., 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.

View all 21 devices →

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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