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New World Medical, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
12
Inspections
5
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K243503VIA360™ Surgical SystemFebruary 14, 2025
K220891Kahook Dual Blade Glide (KDB Glide)May 17, 2024
K230975Ahmed® Glaucoma Valve Model FP7May 12, 2023
K231051Ahmed® Glaucoma Valve Model FP8May 12, 2023
K211680Streamline Surgical SystemOctober 8, 2021
K182518AHMED ClearPath Glaucoma Drainage DeviceJanuary 18, 2019
K171451Ahmed Glaucoma Valve Model FP8August 8, 2017
K162060Ahmed Glaucoma ValveOctober 24, 2016
K060644AHMED GLAUCOMA VALVE, MODEL M4September 18, 2006
K991072AHMED GLAUCOMA VALVE IMPLANTJuly 13, 1999
K980657AHMED GLAUCOMA VALVE, MODEL S3April 20, 1998
K925636AHMED GLAUCOMA VALVE IMPLANTNovember 12, 1993