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FDA 510(k)

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 the device name listed in this FDA 510(k) record. The listed applicant is Encore Medical L.P.. It received FDA 510(k) clearance on 2026-01-15 under 510(k) 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. The listed applicant is Encore Medical L.P.. The 510(k) number is K252567.

When did AltiVate Reverse® ADLC Glenosphere receive FDA 510(k) clearance?

AltiVate Reverse® ADLC Glenosphere received FDA 510(k) clearance on 2026-01-15, under 510(k) number K252567.

Who is the listed applicant for AltiVate Reverse® ADLC Glenosphere?

The FDA 510(k) record lists Encore Medical L.P. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AltiVate Reverse® ADLC Glenosphere?

The FDA product code for AltiVate Reverse® ADLC Glenosphere is PHX.

Other records listing Encore Medical L.P. 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.

K252974EMPOWR KneeK251833EMPOWR Acetabular® Liner ExtensionK252141AltiVate Reverse® GlenoidK251776EMPOWR Revision Knee™ (EMPOWR Revision VVC+, e+ Tibial Insert)K251241EMPOWR Revision Knee™ (EMPOWR Revision Knee™ Symmetric TT Cones)K251184AltiVate Reverse Shoulder System; RSP Shoulder System; SMR Shoulder System; PRIMA Humeral System; PRIMA Glenoid System

View all 31 devices →

Related Devices (Code: PHX)

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.

K260556Veritas Shoulder SystemRestor3DK261683Augment Off-Axis Instrument SystemZimmer, Inc.K260102Tornier Perform Reversed Glenoid and Tornier Perform Reversed Augmented Glenoid Shoulder SystemStryker Corporation (Tornier, Inc.)K261016MSS - Humeral reverse liners extensionMedacta International, SAK253992Veritas Reverse Total Shoulder SystemRestor3DK252404Comprehensive Reverse Shoulder - HA Glenosphere BaseplatesBiomet Orthopedics

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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