ClearanceBrief
Company · US

New World Medical, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1993 to 2025. Name variants (Inc, Corp, punctuation) are merged.

12510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
KYFImplant, Eye Valve9
MRHPump, Infusion, Ophthalmic2
QUQKnife, Intraocular Pressure Lowering1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Feb 14, 2025K243503VIA360™ Surgical System
New World Medical, Inc.
MRH
May 17, 2024K220891Kahook Dual Blade Glide (KDB Glide)
New World Medical, Inc.
QUQ
May 12, 2023K231051Ahmed® Glaucoma Valve Model FP8
New World Medical, Inc.
KYF
May 12, 2023K230975Ahmed® Glaucoma Valve Model FP7
New World Medical, Inc.
KYF
Oct 8, 2021K211680Streamline Surgical System
New World Medical, Inc.
MRH
Jan 18, 2019K182518AHMED ClearPath Glaucoma Drainage Device
New World Medical, Inc.
KYF
Aug 8, 2017K171451Ahmed Glaucoma Valve Model FP8
New World Medical, Inc.
KYF
Oct 24, 2016K162060Ahmed Glaucoma Valve
New World Medical, Inc.
KYF
Sep 18, 2006K060644AHMED GLAUCOMA VALVE, MODEL M4
New World Medical, Inc.
KYF
Jul 13, 1999K991072AHMED GLAUCOMA VALVE IMPLANT
New World Medical, Inc.
KYF
Apr 20, 1998K980657AHMED GLAUCOMA VALVE, MODEL S3
New World Medical, Inc.
KYF
Nov 12, 1993K925636AHMED GLAUCOMA VALVE IMPLANT
New World Medical, Inc.
KYF

Latest recalls

DateFirm and productCodeLinked 510(k)
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