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FDA 510(k)

AURA CERAMIC DENTAL APPLIANCE

K-Number: K902390 · 1990-08-13

ApplicantProgressive Technology, Inc.
Decision Date1990-08-13
Product CodeEJF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

AURA CERAMIC DENTAL APPLIANCE is the device name listed in this FDA 510(k) record. The listed applicant is Progressive Technology, Inc.. It received FDA 510(k) clearance on 1990-08-13 under 510(k) number K902390. The device is classified under product code EJF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AURA CERAMIC DENTAL APPLIANCE?

AURA CERAMIC DENTAL APPLIANCE is a medical device that received FDA 510(k) clearance on 1990-08-13. The listed applicant is Progressive Technology, Inc.. The 510(k) number is K902390.

When did AURA CERAMIC DENTAL APPLIANCE receive FDA 510(k) clearance?

AURA CERAMIC DENTAL APPLIANCE received FDA 510(k) clearance on 1990-08-13, under 510(k) number K902390.

Who is the listed applicant for AURA CERAMIC DENTAL APPLIANCE?

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

What is the FDA product code for AURA CERAMIC DENTAL APPLIANCE?

The FDA product code for AURA CERAMIC DENTAL APPLIANCE is EJF.

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 Progressive Technology, 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.

K812676AMPLITONE-3

Related Devices (Code: EJF)

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.

K994357BITEM LOCK, MODELS SW006, SW012Thermoelastic Technologies, Inc.K932825MICROARCH GOLD BRACKETGac Intl., Inc.K933501ALASTIKUnitek Corp.K923372MEMORY WIREAlthan, Inc.K933080ORTHOTECH DURA-GOLD BARCKETSOrthotechK935139FASCINATION CERAMIC BRACKETDentauraum, Inc.

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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