TEPHAFLEX LIGHT MESH
K-Number: K113721 · 2012-02-15
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Device Summary
Frequently Asked Questions
What is the TEPHAFLEX LIGHT MESH?
TEPHAFLEX LIGHT MESH is a medical device that received FDA 510(k) clearance on 2012-02-15. The listed applicant is Tepha, Inc.. The 510(k) number is K113721.
When did TEPHAFLEX LIGHT MESH receive FDA 510(k) clearance?
TEPHAFLEX LIGHT MESH received FDA 510(k) clearance on 2012-02-15, under 510(k) number K113721.
Who is the listed applicant for TEPHAFLEX LIGHT MESH?
The FDA 510(k) record lists Tepha, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TEPHAFLEX LIGHT MESH?
The FDA product code for TEPHAFLEX LIGHT MESH is OOD.
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 Tepha, 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: OOD)
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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