Allomatrix (Allomatrix Injectable Putty; Allomatrix C; Allomatrix DR; Allomatrix Custom)
K-Number: K252085 · 2025-09-30
Device Summary
Frequently Asked Questions
What is the Allomatrix (Allomatrix Injectable Putty; Allomatrix C; Allomatrix DR; Allomatrix Custom)?
Allomatrix (Allomatrix Injectable Putty; Allomatrix C; Allomatrix DR; Allomatrix Custom) is a medical device that received FDA 510(k) clearance on 2025-09-30. It is manufactured by Wright Medical Technology, Inc. (Stryker Corporation). The 510(k) number is K252085.
When was Allomatrix (Allomatrix Injectable Putty; Allomatrix C; Allomatrix DR; Allomatrix Custom) approved by the FDA?
Allomatrix (Allomatrix Injectable Putty; Allomatrix C; Allomatrix DR; Allomatrix Custom) received FDA 510(k) clearance on 2025-09-30, under approval number K252085.
What company makes Allomatrix (Allomatrix Injectable Putty; Allomatrix C; Allomatrix DR; Allomatrix Custom)?
Allomatrix (Allomatrix Injectable Putty; Allomatrix C; Allomatrix DR; Allomatrix Custom) is manufactured by Wright Medical Technology, Inc. (Stryker Corporation).
What is the FDA product code for Allomatrix (Allomatrix Injectable Putty; Allomatrix C; Allomatrix DR; Allomatrix Custom)?
The FDA product code for Allomatrix (Allomatrix Injectable Putty; Allomatrix C; Allomatrix DR; Allomatrix Custom) is MQV.
Other Devices by Wright Medical Technology, Inc. (Stryker Corporation)
Related Devices (Code: MQV)
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.