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FDA 510(k)

NICKEL-TITANIUM ORTHODONTIC TOOTH SEPARATING SPRIN

K-Number: K902844 · 1990-09-05

ApplicantProgressive Dental Supply
Decision Date1990-09-05
Product CodeEJF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

NICKEL-TITANIUM ORTHODONTIC TOOTH SEPARATING SPRIN is the device name listed in this FDA 510(k) record. The listed applicant is Progressive Dental Supply. It received FDA 510(k) clearance on 1990-09-05 under 510(k) number K902844. 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 NICKEL-TITANIUM ORTHODONTIC TOOTH SEPARATING SPRIN?

NICKEL-TITANIUM ORTHODONTIC TOOTH SEPARATING SPRIN is a medical device that received FDA 510(k) clearance on 1990-09-05. The listed applicant is Progressive Dental Supply. The 510(k) number is K902844.

When did NICKEL-TITANIUM ORTHODONTIC TOOTH SEPARATING SPRIN receive FDA 510(k) clearance?

NICKEL-TITANIUM ORTHODONTIC TOOTH SEPARATING SPRIN received FDA 510(k) clearance on 1990-09-05, under 510(k) number K902844.

Who is the listed applicant for NICKEL-TITANIUM ORTHODONTIC TOOTH SEPARATING SPRIN?

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

What is the FDA product code for NICKEL-TITANIUM ORTHODONTIC TOOTH SEPARATING SPRIN?

The FDA product code for NICKEL-TITANIUM ORTHODONTIC TOOTH SEPARATING SPRIN is EJF.

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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

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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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