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FDA 510(k)

FORESTADENT ORTHODONTIC BANDS

K-Number: K925028 · 1994-01-26

ApplicantForestadent
Decision Date1994-01-26
Product CodeEJF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FORESTADENT ORTHODONTIC BANDS is the device name listed in this FDA 510(k) record. The listed applicant is Forestadent. It received FDA 510(k) clearance on 1994-01-26 under 510(k) number K925028. 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 FORESTADENT ORTHODONTIC BANDS?

FORESTADENT ORTHODONTIC BANDS is a medical device that received FDA 510(k) clearance on 1994-01-26. The listed applicant is Forestadent. The 510(k) number is K925028.

When did FORESTADENT ORTHODONTIC BANDS receive FDA 510(k) clearance?

FORESTADENT ORTHODONTIC BANDS received FDA 510(k) clearance on 1994-01-26, under 510(k) number K925028.

Who is the listed applicant for FORESTADENT ORTHODONTIC BANDS?

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

What is the FDA product code for FORESTADENT ORTHODONTIC BANDS?

The FDA product code for FORESTADENT ORTHODONTIC BANDS 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 Forestadent 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.

K925088EXPANSION SCREWS

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

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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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