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FDA 510(k)

FRI ALIT DENTAL IMPLANT -TUBING

K-Number: K822001 · 1982-08-19

ApplicantFriedrichsfeld GmbH
Decision Date1982-08-19
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FRI ALIT DENTAL IMPLANT -TUBING is the device name listed in this FDA 510(k) record. The listed applicant is Friedrichsfeld GmbH. It received FDA 510(k) clearance on 1982-08-19 under 510(k) number K822001. 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 FRI ALIT DENTAL IMPLANT -TUBING?

FRI ALIT DENTAL IMPLANT -TUBING is a medical device that received FDA 510(k) clearance on 1982-08-19. The listed applicant is Friedrichsfeld GmbH. The 510(k) number is K822001.

When did FRI ALIT DENTAL IMPLANT -TUBING receive FDA 510(k) clearance?

FRI ALIT DENTAL IMPLANT -TUBING received FDA 510(k) clearance on 1982-08-19, under 510(k) number K822001.

Who is the listed applicant for FRI ALIT DENTAL IMPLANT -TUBING?

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

What is the FDA product code for FRI ALIT DENTAL IMPLANT -TUBING?

The FDA product code for FRI ALIT DENTAL IMPLANT -TUBING is DZE.

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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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