Home › Device types › LFB
Button, Nasal Septal
FDA product code LFB · Class U · Unknown
50
Registered devices
7
Adverse events
2
Recalls
12
510(k) clearances
Devices with this code
InHealth Technologies; Blom-Singer — Freudenberg Medical, LLCNasal Septal Button — Boston Medical Products, Inc.Hood Nasal Septal Button — HOOD, E BENSON LABORATORIES INCHood Nasal Septal Button — HOOD, E BENSON LABORATORIES INCHood Nasal Septal Button — HOOD, E BENSON LABORATORIES INCInHealth Technologies; Blom-Singer — Freudenberg Medical, LLCInHealth Technologies; Blom-Singer — Freudenberg Medical, LLCInHealth Technologies; Blom-Singer — Freudenberg Medical, LLCInHealth Technologies; Blom-Singer — Freudenberg Medical, LLCInHealth Technologies; Blom-Singer — Freudenberg Medical, LLCInHealth Technologies; Blom-Singer — Freudenberg Medical, LLCSUMMIT MEDICAL — Summit Medical, Inc.NA — MEDTRONIC XOMED, INC.Hood Nasal Septal Button — HOOD, E BENSON LABORATORIES INCHood Nasal Septal Button — HOOD, E BENSON LABORATORIES INCN/A — MEDTRONIC XOMED, INC.InHealth Technologies; Blom-Singer — Freudenberg Medical, LLCInHealth Technologies; Blom-Singer — Freudenberg Medical, LLCNA — Summit Medical, Inc.NA — MEDTRONIC XOMED, INC.Invotec Nasal Septal Button — INVOTEC INTERNATIONAL, INC.InHealth Technologies; Blom-Singer — Freudenberg Medical, LLCN/A — MEDTRONIC XOMED, INC.InHealth Technologies; Blom-Singer — Freudenberg Medical, LLC
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2023-01-13 | Summit Medical, LLC | Sterile product pouches were not sealed. |
| 2010-03-15 | Micromedics, Inc. | Micromedics, Inc is conducting a product recall on a number of medical device products because of weak seals of the sterile pouches, potentially resulting in a |
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