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Punch, Corneo-Scleral

FDA product code HNJ · Class 1 · Ophthalmic

184
Registered devices
12
Adverse events
1
Recalls
3
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2013-06-27Insight 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

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.