FACEBOW
K-Number: K980195 · 1998-03-11
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Device Summary
Frequently Asked Questions
What is the FACEBOW?
FACEBOW is a medical device that received FDA 510(k) clearance on 1998-03-11. The listed applicant is Ortho Kinetics Corp.. The 510(k) number is K980195.
When did FACEBOW receive FDA 510(k) clearance?
FACEBOW received FDA 510(k) clearance on 1998-03-11, under 510(k) number K980195.
Who is the listed applicant for FACEBOW?
The FDA 510(k) record lists Ortho Kinetics Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FACEBOW?
The FDA product code for FACEBOW is DZB.
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 Ortho Kinetics Corp. 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: DZB)
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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