FDA Device Intelligence
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Curette, Ear

FDA product code JYG · Class 1 · Ear, Nose, Throat

1,598
Registered devices
27
Adverse events
1
Recalls
7
510(k) clearances

Devices with this code

PILLING — TELEFLEX INCORPORATEDNovo Surgical — NOVO SURGICAL, INC.BEAR — Mytamed, Inc.Beckmann adenoid curette — Spiggle & Theis Medizintechnik GmbHAESCULAP — Aesculap AGNegus adenoid curette — Spiggle & Theis Medizintechnik GmbHSpoon curette — Spiggle & Theis Medizintechnik GmbHSymmetry Surgical — ASPEN SURGICAL PRODUCTS, INC.Symmetry Rosen — ASPEN SURGICAL PRODUCTS, INC.Millennium — Avalign Technologies, Inc.Medicon — Medicon eG. Chirurgiemechaniker-GenossenschaftJobson Horne Probe - Sterile — ADEPT MEDICAL LIMITEDMillennium — Avalign Technologies, Inc.PILLING — TELEFLEX INCORPORATEDBUCK EAR CURETTE — SONTEC INSTRUMENTS, INC.Ambler Surgical — AMBLER SURGICAL CORP.BEAR — Bear-Ent, LLCCurette — Spiggle & Theis Medizintechnik GmbHSklar — SKLAR CORPORATIONIntegra® Miltex® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONBR Surgical, LLC — BR Surgical, LLCTisch micro curette — Spiggle & Theis Medizintechnik GmbHNegus adenoid curette — Spiggle & Theis Medizintechnik GmbHBuck ear curette — Spiggle & Theis Medizintechnik GmbH

Recent recalls

DateFirmReason
2024-12-03Sklar InstrumentsReports of various packaging issues that may result in a breach of the sterile barrier.

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