FDA Device Intelligence
Home › Device types › FBX

Sound, Urethral, Metal Or Plastic

FDA product code FBX · Class 1 · Gastroenterology, Urology

1,337
Registered devices
16
Adverse events
1
Recalls
1
510(k) clearances

Devices with this code

Integra® Miltex® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONMedicon — Medicon eG. Chirurgiemechaniker-GenossenschaftNovo Surgical Inc. — NOVO SURGICAL, INC.AESCULAP — AESCULAP, INC.Hayden Medical — Hayden Medical, Inc.Symmetry Mccrea — ASPEN SURGICAL PRODUCTS, INC.Novo Surgical — NOVO SURGICAL, INC.BR Surgical, LLC — BR Surgical, LLCSklar® — SKLAR CORPORATIONIntegra® Jarit® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONNovo Surgical Inc. — NOVO SURGICAL, INC.Integra® Jarit® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONMSI Precision Specialty Instruments — Med Saver, Inc.Integra® Miltex® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONMedicon — Medicon eG. Chirurgiemechaniker-GenossenschaftPILLING — TELEFLEX INCORPORATEDGreenwald Surgical Company, Inc. — GRACE MANUFACTURING, INC.PILLING — TELEFLEX INCORPORATEDIntegra® Jarit® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONKMEDIC — TELEFLEX INCORPORATEDMSI Precision Specialty Instruments — Med Saver, Inc.Integra® Jarit® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONAESCULAP — AESCULAP, INC.Medicon — Medicon eG. Chirurgiemechaniker-Genossenschaft

Recent recalls

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

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