Home › Device types › HNJ
Punch, Corneo-Scleral
FDA product code HNJ · Class 1 · Ophthalmic
185
Registered devices
12
Adverse events
1
Recalls
3
510(k) clearances
Devices with this code
MSI Precision Specialty Instruments — Med Saver, Inc.ONE — MORIA SASURGISTAR — SURGISTAR, INC.ONE — MORIA SATrab. Punch — KATENA PRODUCTS, INC.ONE — MORIA SAPunches — AURORA SURGICAL, LLCMSI Precision Specialty Instruments — Med Saver, Inc.MSI Precision Specialty Instruments — Med Saver, Inc.ONE — MORIA SAMSI Precision Specialty Instruments — Med Saver, Inc.MORIA — MORIA SAONE — MORIA SAMSI Precision Specialty Instruments — Med Saver, Inc.ONE — MORIA SAONE — MORIA SAONE — MORIA SAMILLENNIUM — Avalign Technologies, Inc.Ambler Surgical — AMBLER SURGICAL CORP.Ambler Surgical — AMBLER SURGICAL CORP.Wexler Surgical, Inc. — WEXLER SURGICAL, INC.ONE — MORIA SAMSI Precision Specialty Instruments — Med Saver, Inc.Rumex — RUMEX INTERNATIONAL CORP.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2013-06-27 | Insight Instruments, Inc. | The product was registered and distributed as a Class I medical device and was subsequently determined to be a Class II medical device which requires FDA market |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.
