Home › Device types › EMX
Balloon, Epistaxis
FDA product code EMX · Class 1 · Ear, Nose, Throat
368
Registered devices
102
Adverse events
4
Recalls
47
510(k) clearances
Devices with this code
OSSEOUS — EON MEDITECH PRIVATE LIMITEDFABCO — FIRST AID BANDAGE CO INCRapid Rhino — Smith & Nephew, Inc.Epi-Max™ Epistaxis Catheter — Boston Medical Products, Inc.Ultracell® — Beaver-Visitec International, Inc.DeRoyal — DEROYAL INDUSTRIES, INC.Ultracell® — Beaver-Visitec International, Inc.Epistax Balloon Catheter — Summit Medical, Inc.Gyrus ACMI — Gyrus ACMI, LLCRHINOCELL® Nasal Packing — Boston Medical Products, Inc.Epistax Balloon Catheter — Summit Medical, Inc.OSSEOUS — EON MEDITECH PRIVATE LIMITEDOSSEOUS — EON MEDITECH PRIVATE LIMITEDGyrus ACMI — Gyrus ACMI, LLCOSSEOUS — EON MEDITECH PRIVATE LIMITEDEpistat® — MEDTRONIC XOMED, INC.Ultracell® — Beaver-Visitec International, Inc.Epistax Balloon Catheter — Summit Medical, Inc.Epistax Balloon Catheter — Summit Medical, Inc.Ultracell® — Beaver-Visitec International, Inc.OSSEOUS — EON MEDITECH PRIVATE LIMITEDOSSEOUS — EON MEDITECH PRIVATE LIMITEDPosiSep C 0.6 x 2.0 — HEMOSTASIS, LLCDeRoyal — DEROYAL INDUSTRIES, INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2003-01-08 | Ultracell Medical Technologies | Sterility of the device is compromised |
| 2003-01-08 | Ultracell Medical Technologies | Sterility of the device is compromised |
| 2003-01-08 | Ultracell Medical Technologies | Sterility of the device is compromised |
| 2003-01-08 | Ultracell Medical Technologies | Sterility of the device is compromised |
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.