Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

LANCER ORIGINAL, SIERRA, GENERAL PURPOSE

K-Number: K904092 · 1990-11-09

ApplicantLancer Orthodontics, Inc.
Decision Date1990-11-09
Product CodeEJF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LANCER ORIGINAL, SIERRA, GENERAL PURPOSE is the device name listed in this FDA 510(k) record. The listed applicant is Lancer Orthodontics, Inc.. It received FDA 510(k) clearance on 1990-11-09 under 510(k) number K904092. 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 LANCER ORIGINAL, SIERRA, GENERAL PURPOSE?

LANCER ORIGINAL, SIERRA, GENERAL PURPOSE is a medical device that received FDA 510(k) clearance on 1990-11-09. The listed applicant is Lancer Orthodontics, Inc.. The 510(k) number is K904092.

When did LANCER ORIGINAL, SIERRA, GENERAL PURPOSE receive FDA 510(k) clearance?

LANCER ORIGINAL, SIERRA, GENERAL PURPOSE received FDA 510(k) clearance on 1990-11-09, under 510(k) number K904092.

Who is the listed applicant for LANCER ORIGINAL, SIERRA, GENERAL PURPOSE?

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

What is the FDA product code for LANCER ORIGINAL, SIERRA, GENERAL PURPOSE?

The FDA product code for LANCER ORIGINAL, SIERRA, GENERAL PURPOSE 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 Lancer Orthodontics, 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.

K122069STORM MINI SCREWK071192BLUGOO HDK051552O.A.S.I. SYSTEMK991481PARAGONK904090ORTHODONTIC BONDING ADHESIVE CONTROLK904093BUCCAL TUBE, BUCCAL ATTACHMENT

View all 14 devices →

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.

↑