New World Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
New World Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: VIA360™ Surgical System, Kahook Dual Blade Glide (KDB Glide), Ahmed® Glaucoma Valve Model FP7
12
Total
12
Cleared
0
Denied
New World Medical, Inc. has 12 FDA 510(k) cleared ophthalmic devices. Based in Rancho Cucamonga, US.
Latest FDA clearance: Feb 2025. Active since 1993.
Browse the complete list of FDA 510(k) cleared ophthalmic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - New World Medical, Inc.
12 devices
Cleared
Feb 14, 2025
VIA360™ Surgical System
Ophthalmic
94d
Cleared
May 17, 2024
Kahook Dual Blade Glide (KDB Glide)
Ophthalmic
781d
Cleared
May 12, 2023
Ahmed® Glaucoma Valve Model FP7
Ophthalmic
37d
Cleared
May 12, 2023
Ahmed® Glaucoma Valve Model FP8
Ophthalmic
29d
Cleared
Oct 08, 2021
Streamline Surgical System
Ophthalmic
129d
Cleared
Jan 18, 2019
AHMED ClearPath Glaucoma Drainage Device
Ophthalmic
127d
Cleared
Aug 08, 2017
Ahmed Glaucoma Valve Model FP8
Ophthalmic
83d
Cleared
Oct 24, 2016
Ahmed Glaucoma Valve
Ophthalmic
90d
Cleared
Sep 18, 2006
AHMED GLAUCOMA VALVE, MODEL M4
Ophthalmic
192d
Cleared
Jul 13, 1999
AHMED GLAUCOMA VALVE IMPLANT
Ophthalmic
104d
Cleared
Apr 20, 1998
AHMED GLAUCOMA VALVE, MODEL S3
Ophthalmic
74d
Cleared
Nov 12, 1993
AHMED GLAUCOMA VALVE IMPLANT
Ophthalmic
368d