Remanufactured EndoWrist Cadiere Forceps (420049)
K-Number: K250399 · 2025-08-19
ApplicantRebotix
Decision Date2025-08-19
Product CodeQSM
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
Remanufactured EndoWrist Cadiere Forceps (420049) is a medical device manufactured by Rebotix. It received FDA 510(k) clearance on 2025-08-19 under approval number K250399. The device is classified under product code QSM. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Remanufactured EndoWrist Cadiere Forceps (420049)?
Remanufactured EndoWrist Cadiere Forceps (420049) is a medical device that received FDA 510(k) clearance on 2025-08-19. It is manufactured by Rebotix. The 510(k) number is K250399.
When was Remanufactured EndoWrist Cadiere Forceps (420049) approved by the FDA?
Remanufactured EndoWrist Cadiere Forceps (420049) received FDA 510(k) clearance on 2025-08-19, under approval number K250399.
What company makes Remanufactured EndoWrist Cadiere Forceps (420049)?
Remanufactured EndoWrist Cadiere Forceps (420049) is manufactured by Rebotix.
What is the FDA product code for Remanufactured EndoWrist Cadiere Forceps (420049)?
The FDA product code for Remanufactured EndoWrist Cadiere Forceps (420049) is QSM.
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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.