Home › Device types › NOC
Splint, Extremity, Non-Inflatable, External, Non-Sterile
FDA product code NOC · Class 1 · General, Plastic Surgery
421
Registered devices
13
Adverse events
1
Recalls
0
510(k) clearances
Devices with this code
Health Design Tall Leg Walker — DARCO INTERNATIONAL, INC.DARCO® Body Armor® Walker II — DARCO INTERNATIONAL, INC.MORRISON MEDICAL — MORRISON MEDICAL, LTDMORRISON MEDICAL — MORRISON MEDICAL, LTDRedi Splint — FARETEC, INC.Spencer — SPENCER ITALIA SRLSAM Splint — SAM Medical ProductsMORRISON MEDICAL — MORRISON MEDICAL, LTDDARCO® Relief Insert™ Walker — Darco (Europe) GmbHHealth Design Ankle Leg Walker — DARCO INTERNATIONAL, INC.SAM Splint XL — SAM Medical ProductsDARCO® Body Armor® Walker liner — DARCO INTERNATIONAL, INC.DARCO® Body Armor® Walker II — DARCO INTERNATIONAL, INC.Redi Splint — FARETEC, INC.DARCO® FX Pro™ Walker — DARCO INTERNATIONAL, INC.DARCO® Body Armor® Walker II — DARCO INTERNATIONAL, INC.Dynarex ActiSplint — Dynarex CorporationDARCO® Night Splint — DARCO INTERNATIONAL, INC.MORRISON MEDICAL — MORRISON MEDICAL, LTDRedi Splint — FARETEC, INC.Redi Splint — FARETEC, INC.RISE Splint — TACTICAL MEDICAL SOLUTIONS, LLCDARCO® Relief Insert™ — Darco (Europe) GmbHRedi Splint 2 — FARETEC, INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2017-11-01 | 3M Company - Health Care Business | Mold was found on the non-patient contact surfaces of the product and was identified as Aspergillus candidus. |
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