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Probe, Rectal, Non-Powered

FDA product code EXX · Class 1 · Gastroenterology, Urology

65
Registered devices
10
Adverse events
1
Recalls
0
510(k) clearances

Devices with this code

Integra® Jarit® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONAmbler Surgical — AMBLER SURGICAL CORP.Medicon — Medicon eG. Chirurgiemechaniker-GenossenschaftNovo Surgical Inc. — NOVO SURGICAL, INC.Integra® Miltex® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONGimmi — Gimmi GmbHNovo Surgical Inc. — NOVO SURGICAL, INC.GreenEgg — Endoglow, LLCNovo Surgical — NOVO SURGICAL, INC.Integra® Jarit® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONMarina Medical — MARINA MEDICAL INSTRUMENTS, INC.Marina Medical — MARINA MEDICAL INSTRUMENTS, INC.Marina Medical — MARINA MEDICAL INSTRUMENTS, INC.Integra® Jarit® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONNovo Surgical Inc. — NOVO SURGICAL, INC.Medicon — Medicon eG. Chirurgiemechaniker-GenossenschaftIntegra® Miltex® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONIntegra® Jarit® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONMedicon — Medicon eG. Chirurgiemechaniker-GenossenschaftNovo Surgical Inc. — NOVO SURGICAL, INC.Marina Medical — MARINA MEDICAL INSTRUMENTS, INC.Integra® Miltex® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONMSI Precision Specialty Instruments — Med Saver, Inc.Novo Surgical — NOVO SURGICAL, INC.

Recent recalls

DateFirmReason
2009-04-09Marina Medical Instruments Inc.Marina Medical, Sunrise, FL initiated recall of 46 different 350 series devices and 47 different 270 series products because the material used to manufacture th

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