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FDA 510(k)

TITANAL,STERLING SPRING,DUAL FLEX,MEMOREX,BENDALLO

K-Number: K904091 · 1990-11-05

ApplicantLancer Orthodontics, Inc.
Decision Date1990-11-05
Product CodeEJF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TITANAL,STERLING SPRING,DUAL FLEX,MEMOREX,BENDALLO 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 1990-11-05 under 510(k) number K904091. 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 TITANAL,STERLING SPRING,DUAL FLEX,MEMOREX,BENDALLO?

TITANAL,STERLING SPRING,DUAL FLEX,MEMOREX,BENDALLO is a medical device that received FDA 510(k) clearance on 1990-11-05. The listed applicant is Lancer Orthodontics, Inc.. The 510(k) number is K904091.

When did TITANAL,STERLING SPRING,DUAL FLEX,MEMOREX,BENDALLO receive FDA 510(k) clearance?

TITANAL,STERLING SPRING,DUAL FLEX,MEMOREX,BENDALLO received FDA 510(k) clearance on 1990-11-05, under 510(k) number K904091.

Who is the listed applicant for TITANAL,STERLING SPRING,DUAL FLEX,MEMOREX,BENDALLO?

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 TITANAL,STERLING SPRING,DUAL FLEX,MEMOREX,BENDALLO?

The FDA product code for TITANAL,STERLING SPRING,DUAL FLEX,MEMOREX,BENDALLO is EJF.

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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.

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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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