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FDA 510(k)

APACERAM HYDROXYLAPATITE DENTAL IMPLANT (TYPE G)

K-Number: K872089 · 1987-08-14

Decision Date1987-08-14
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

APACERAM HYDROXYLAPATITE DENTAL IMPLANT (TYPE G) is the device name listed in this FDA 510(k) record. The listed applicant is Asahi Optical Co. C/O Rosati Associates, P.C.. It received FDA 510(k) clearance on 1987-08-14 under 510(k) number K872089. 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 APACERAM HYDROXYLAPATITE DENTAL IMPLANT (TYPE G)?

APACERAM HYDROXYLAPATITE DENTAL IMPLANT (TYPE G) is a medical device that received FDA 510(k) clearance on 1987-08-14. The listed applicant is Asahi Optical Co. C/O Rosati Associates, P.C.. The 510(k) number is K872089.

When did APACERAM HYDROXYLAPATITE DENTAL IMPLANT (TYPE G) receive FDA 510(k) clearance?

APACERAM HYDROXYLAPATITE DENTAL IMPLANT (TYPE G) received FDA 510(k) clearance on 1987-08-14, under 510(k) number K872089.

Who is the listed applicant for APACERAM HYDROXYLAPATITE DENTAL IMPLANT (TYPE G)?

The FDA 510(k) record lists Asahi Optical Co. C/O Rosati Associates, P.C. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for APACERAM HYDROXYLAPATITE DENTAL IMPLANT (TYPE G)?

The FDA product code for APACERAM HYDROXYLAPATITE DENTAL IMPLANT (TYPE G) 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 Asahi Optical Co. C/O Rosati Associates, P.C. 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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