Laon Ortho
K-Number: K250198 · 2025-04-23
ApplicantLaon Medi, Inc.
Decision Date2025-04-23
Product CodePNN
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Laon Ortho is a medical device manufactured by Laon Medi, Inc.. It received FDA 510(k) clearance on 2025-04-23 under approval number K250198. The device is classified under product code PNN. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Laon Ortho?
Laon Ortho is a medical device that received FDA 510(k) clearance on 2025-04-23. It is manufactured by Laon Medi, Inc.. The 510(k) number is K250198.
When was Laon Ortho approved by the FDA?
Laon Ortho received FDA 510(k) clearance on 2025-04-23, under approval number K250198.
What company makes Laon Ortho?
Laon Ortho is manufactured by Laon Medi, Inc..
What is the FDA product code for Laon Ortho?
The FDA product code for Laon Ortho is PNN.
Other Devices by Laon Medi, Inc.
Related Devices (Code: PNN)
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.