ADHESIVE, BRACKET AND CONDITIONER RESIN
K-Number: K780334 · 1978-03-28
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Device Summary
Frequently Asked Questions
What is the ADHESIVE, BRACKET AND CONDITIONER RESIN?
ADHESIVE, BRACKET AND CONDITIONER RESIN is a medical device that received FDA 510(k) clearance on 1978-03-28. The listed applicant is Rocky Mountain Orthodontics, Inc.. The 510(k) number is K780334.
When did ADHESIVE, BRACKET AND CONDITIONER RESIN receive FDA 510(k) clearance?
ADHESIVE, BRACKET AND CONDITIONER RESIN received FDA 510(k) clearance on 1978-03-28, under 510(k) number K780334.
Who is the listed applicant for ADHESIVE, BRACKET AND CONDITIONER RESIN?
The FDA 510(k) record lists Rocky Mountain Orthodontics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ADHESIVE, BRACKET AND CONDITIONER RESIN?
The FDA product code for ADHESIVE, BRACKET AND CONDITIONER RESIN is DYH.
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.
Other records listing Rocky Mountain 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.
Related Devices (Code: DYH)
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.
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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