AltiVate Reverse® ADLC Glenosphere
K-Number: K252567 · 2026-01-15
ApplicantEncore Medical L.P.
Decision Date2026-01-15
Product CodePHX
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
AltiVate Reverse® ADLC Glenosphere is a medical device manufactured by Encore Medical L.P.. It received FDA 510(k) clearance on 2026-01-15 under approval number K252567. The device is classified under product code PHX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the AltiVate Reverse® ADLC Glenosphere?
AltiVate Reverse® ADLC Glenosphere is a medical device that received FDA 510(k) clearance on 2026-01-15. It is manufactured by Encore Medical L.P.. The 510(k) number is K252567.
When was AltiVate Reverse® ADLC Glenosphere approved by the FDA?
AltiVate Reverse® ADLC Glenosphere received FDA 510(k) clearance on 2026-01-15, under approval number K252567.
What company makes AltiVate Reverse® ADLC Glenosphere?
AltiVate Reverse® ADLC Glenosphere is manufactured by Encore Medical L.P..
What is the FDA product code for AltiVate Reverse® ADLC Glenosphere?
The FDA product code for AltiVate Reverse® ADLC Glenosphere is PHX.
Other Devices by Encore Medical L.P.
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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.