Home › Device types › EMX
Balloon, Epistaxis
FDA product code EMX · Class 1 · Ear, Nose, Throat
368
Registered devices
103
Adverse events
4
Recalls
47
510(k) clearances
Devices with this code
OSSEOUS — EON MEDITECH PRIVATE LIMITEDOSSEOUS — EON MEDITECH PRIVATE LIMITEDPosiSep X2 0.7" x 1.7" — HEMOSTASIS, LLCUltracell® — Beaver-Visitec International, Inc.Ultracell — Beaver-Visitec International, Inc.Gyrus ACMI — Gyrus ACMI, LLCRapid Rhino — Smith & Nephew, Inc.FABCO — FIRST AID BANDAGE CO INCExpanding epistaxis nasal tampon — Spiggle & Theis Medizintechnik GmbHDeRoyal — DEROYAL INDUSTRIES, INC.OSSEOUS — EON MEDITECH PRIVATE LIMITEDOSSEOUS — EON MEDITECH PRIVATE LIMITEDNasal Sponges Sterile — Dynarex CorporationOSSEOUS — EON MEDITECH PRIVATE LIMITEDPosiSep X 0.6 x 2.0 Hemostatic Dressing/Intranasal Splint — HEMOSTASIS, LLCSlimLine — Gyrus ACMI, LLCOSSEOUS — EON MEDITECH PRIVATE LIMITEDOSSEOUS — EON MEDITECH PRIVATE LIMITEDRapid Rhino — Smith & Nephew, Inc.Gyrus ACMI — Gyrus ACMI, LLCEpistax Balloon Catheter — Summit Medical, Inc.PosiSep C — HEMOSTASIS, LLCOSSEOUS — EON MEDITECH PRIVATE LIMITEDEpistax Balloon Catheter — Summit Medical, 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 |
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