ENCORE TONGUE SUSPENSION SYSTEM
K-Number: K121814 · 2012-11-07
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Device Summary
Frequently Asked Questions
What is the ENCORE TONGUE SUSPENSION SYSTEM?
ENCORE TONGUE SUSPENSION SYSTEM is a medical device that received FDA 510(k) clearance on 2012-11-07. The listed applicant is Siesta Medical, Inc.. The 510(k) number is K121814.
When did ENCORE TONGUE SUSPENSION SYSTEM receive FDA 510(k) clearance?
ENCORE TONGUE SUSPENSION SYSTEM received FDA 510(k) clearance on 2012-11-07, under 510(k) number K121814.
Who is the listed applicant for ENCORE TONGUE SUSPENSION SYSTEM?
The FDA 510(k) record lists Siesta Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ENCORE TONGUE SUSPENSION SYSTEM?
The FDA product code for ENCORE TONGUE SUSPENSION SYSTEM is ORY.
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 Siesta Medical, 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: ORY)
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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