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FDA 510(k)

TRI-STAGE (TS-I) DENTAL IMPLANT

K-Number: K880220 · 1988-03-31

ApplicantTri-Stage, Inc.
Decision Date1988-03-31
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TRI-STAGE (TS-I) DENTAL IMPLANT is the device name listed in this FDA 510(k) record. The listed applicant is Tri-Stage, Inc.. It received FDA 510(k) clearance on 1988-03-31 under 510(k) number K880220. 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 TRI-STAGE (TS-I) DENTAL IMPLANT?

TRI-STAGE (TS-I) DENTAL IMPLANT is a medical device that received FDA 510(k) clearance on 1988-03-31. The listed applicant is Tri-Stage, Inc.. The 510(k) number is K880220.

When did TRI-STAGE (TS-I) DENTAL IMPLANT receive FDA 510(k) clearance?

TRI-STAGE (TS-I) DENTAL IMPLANT received FDA 510(k) clearance on 1988-03-31, under 510(k) number K880220.

Who is the listed applicant for TRI-STAGE (TS-I) DENTAL IMPLANT?

The FDA 510(k) record lists Tri-Stage, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TRI-STAGE (TS-I) DENTAL IMPLANT?

The FDA product code for TRI-STAGE (TS-I) DENTAL IMPLANT is DZE.

Related Clinical Trials

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Other records listing Tri-Stage, 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.

K882834TISSUE PUNCHK882183DENTAL BURS

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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