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FDA 510(k)

LAMINOSS DENTAL IMPLANT

K-Number: K933705 · 1996-06-24

ApplicantImpladent , Ltd.
Decision Date1996-06-24
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LAMINOSS DENTAL IMPLANT is the device name listed in this FDA 510(k) record. The listed applicant is Impladent , Ltd.. It received FDA 510(k) clearance on 1996-06-24 under 510(k) number K933705. 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 LAMINOSS DENTAL IMPLANT?

LAMINOSS DENTAL IMPLANT is a medical device that received FDA 510(k) clearance on 1996-06-24. The listed applicant is Impladent , Ltd.. The 510(k) number is K933705.

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

LAMINOSS DENTAL IMPLANT received FDA 510(k) clearance on 1996-06-24, under 510(k) number K933705.

Who is the listed applicant for LAMINOSS DENTAL IMPLANT?

The FDA 510(k) record lists Impladent , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LAMINOSS DENTAL IMPLANT?

The FDA product code for LAMINOSS 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Impladent , Ltd. 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.

K090794OSTEOTAPEK033098OSTEOGEN SBRGK982925LAMINOSS DENTAL IMPLANT

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.

K261392TriActive Dental Implant SystemParagon Implant Mfg., LLCK260463ZEROS Dental Implant SystemZeros Co., Ltd.K251188UNIQA® Dental Implants SystemUniqa Dental, Ltd.K251232MegaGen Zygoma Dental Implant SystemMegagen Implant Co., Ltd.K250806Dental Implant SystemA.B. Dental Devices , Ltd.K260006INOSS SystemInosys, Inc.

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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