MANDIBULAR LIP BUMPER AND LIP BUMPER TUBES
K-Number: K891775 · 1989-05-11
Advertisement
Device Summary
Frequently Asked Questions
What is the MANDIBULAR LIP BUMPER AND LIP BUMPER TUBES?
MANDIBULAR LIP BUMPER AND LIP BUMPER TUBES is a medical device that received FDA 510(k) clearance on 1989-05-11. The listed applicant is American Orthodontics. The 510(k) number is K891775.
When did MANDIBULAR LIP BUMPER AND LIP BUMPER TUBES receive FDA 510(k) clearance?
MANDIBULAR LIP BUMPER AND LIP BUMPER TUBES received FDA 510(k) clearance on 1989-05-11, under 510(k) number K891775.
Who is the listed applicant for MANDIBULAR LIP BUMPER AND LIP BUMPER TUBES?
The FDA 510(k) record lists American Orthodontics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MANDIBULAR LIP BUMPER AND LIP BUMPER TUBES?
The FDA product code for MANDIBULAR LIP BUMPER AND LIP BUMPER TUBES 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.
Other records listing American Orthodontics 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: 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.
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.
Advertisement