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FDA 510(k)

MTS Gepotidacin 0.016-256 µg/mL

K-Number: K260696 · 2026-04-17

Decision Date2026-04-17
Product CodeJWY
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MTS Gepotidacin 0.016-256 µg/mL is a medical device manufactured by Liofilchem s.r.l.. It received FDA 510(k) clearance on 2026-04-17 under approval number K260696. The device is classified under product code JWY. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MTS Gepotidacin 0.016-256 µg/mL?

MTS Gepotidacin 0.016-256 µg/mL is a medical device that received FDA 510(k) clearance on 2026-04-17. It is manufactured by Liofilchem s.r.l.. The 510(k) number is K260696.

When was MTS Gepotidacin 0.016-256 µg/mL approved by the FDA?

MTS Gepotidacin 0.016-256 µg/mL received FDA 510(k) clearance on 2026-04-17, under approval number K260696.

What company makes MTS Gepotidacin 0.016-256 µg/mL?

MTS Gepotidacin 0.016-256 µg/mL is manufactured by Liofilchem s.r.l..

What is the FDA product code for MTS Gepotidacin 0.016-256 µg/mL?

The FDA product code for MTS Gepotidacin 0.016-256 µg/mL is JWY.

Other Devices by Liofilchem s.r.l.

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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.