# New World Medical, Inc.

- Location (FDA's records): Rancho Cucamonga, CA
- FDA decisions: 12 (1993–2025): 12 510(k) clearances
- Product codes: KYF (9), MRH (2), QUQ (1)
- Predicates its devices cite: 14 (6 its own); citations of its devices by later devices: 8 (6 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Wright Medical Corp.: 2 (https://510kreport.com/company/wright-medical)
- Staar Surgical Co.: 2 (https://510kreport.com/company/staar-surgical)
- Sight Sciences, Inc.: 2 (https://510kreport.com/company/sight-sciences)
- Neomedix Corp.: 1 (https://510kreport.com/company/neomedix)
- Pharmacia Iovision, Inc.: 1 (https://510kreport.com/company/pharmacia-iovision)

## Firms that cite its devices most
- Allergan, Inc.: 1 (https://510kreport.com/company/allergan)
- Optonol, Ltd.: 1 (https://510kreport.com/company/optonol)

## Its most-cited devices
- K925636: Ahmed Glaucoma Valve Implant (1993), cited by 3
- K162060: Ahmed Glaucoma Valve (2016), cited by 2
- K980657: Ahmed Glaucoma Valve, Model S3 (1998), cited by 2
- K171451: Ahmed Glaucoma Valve Model FP8 (2017), cited by 1

## Recent decisions
- K243503: VIA360™ Surgical System (Feb 14, 2025)
- K220891: Kahook Dual Blade Glide (KDB Glide) (May 17, 2024)
- K230975: Ahmed® Glaucoma Valve Model FP7 (May 12, 2023)
- K231051: Ahmed® Glaucoma Valve Model FP8 (May 12, 2023)
- K211680: Streamline Surgical System (Oct 8, 2021)
- K182518: AHMED ClearPath Glaucoma Drainage Device (Jan 18, 2019)
- K171451: Ahmed Glaucoma Valve Model FP8 (Aug 8, 2017)
- K162060: Ahmed Glaucoma Valve (Oct 24, 2016)

Source page: https://510kreport.com/company/new-world-medical