New World Medical, Inc.
Rancho Cucamonga, CA, US
New World Medical, Inc. appears in FDA device records in Rancho Cucamonga, CA. FDA records list 12 510(k) clearances between and , no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.
FDA records held for this company
510(k) clearance history
FDA records hold 12 510(k) clearances for New World Medical, Inc. between 1993 and 2025. The busiest year on record is 2023, with 2. The most recent is 2025, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1993 | 1 |
| 1998 | 1 |
| 1999 | 1 |
| 2006 | 1 |
| 2016 | 1 |
| 2017 | 1 |
| 2019 | 1 |
| 2021 | 1 |
| 2023 | 2 |
| 2024 | 1 |
| 2025 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K243503 | VIA360™ Surgical System | MRH | Substantially Equivalent | |
| K220891 | Kahook Dual Blade Glide (KDB Glide) | QUQ | Substantially Equivalent | |
| K231051 | Ahmed® Glaucoma Valve Model FP8 | KYF | Substantially Equivalent | |
| K230975 | Ahmed® Glaucoma Valve Model FP7 | KYF | Substantially Equivalent | |
| K211680 | Streamline Surgical System | MRH | Substantially Equivalent | |
| K182518 | AHMED ClearPath Glaucoma Drainage Device | KYF | Substantially Equivalent | |
| K171451 | Ahmed Glaucoma Valve Model FP8 | KYF | Substantially Equivalent | |
| K162060 | Ahmed Glaucoma Valve | KYF | Substantially Equivalent | |
| K060644 | AHMED GLAUCOMA VALVE, MODEL M4 | KYF | Substantially Equivalent | |
| K991072 | AHMED GLAUCOMA VALVE IMPLANT | KYF | Substantially Equivalent | |
| K980657 | AHMED GLAUCOMA VALVE, MODEL S3 | KYF | Substantially Equivalent | |
| K925636 | AHMED GLAUCOMA VALVE IMPLANT | KYF | Substantially Equivalent |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 1000125279 | 1000125279 | New World Medical, Inc. | 10763 Edison Court, Rancho Cucamonga, CA 91730 US | 2026 |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain