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
DARCO® Relief Insert™ Walker 2.0 Lining — Darco (Europe) GmbHMaster — Dongguan Maisite Medical Instruments Co., Ltd.DARCO® Night Splint — DARCO INTERNATIONAL, INC.DARCO® Relief Insert™ Walker Customized — Darco (Europe) GmbHRedi Splint — FARETEC, INC.SAM Splint XL — SAM Medical ProductsSAM Splint — SAM Medical ProductsDARCO® Night Splint — DARCO INTERNATIONAL, INC.MORRISON MEDICAL — MORRISON MEDICAL, LTDMORRISON MEDICAL — MORRISON MEDICAL, LTDMORRISON MEDICAL — MORRISON MEDICAL, LTDMORRISON MEDICAL — MORRISON MEDICAL, LTDMORRISON MEDICAL — MORRISON MEDICAL, LTDMORRISON MEDICAL — MORRISON MEDICAL, LTDBody Armor® Stirrup Walker — DARCO INTERNATIONAL, INC.DARCO® Relief Insert™ Walker — Darco (Europe) GmbHMORRISON MEDICAL — MORRISON MEDICAL, LTDSAM Splint — SAM Medical ProductsSpencer — SPENCER ITALIA SRLDARCO® Toe Plate — DARCO INTERNATIONAL, INC.Redi Splint — FARETEC, INC.KENTEX — KENTRON HEALTHCARE, INC.MORRISON MEDICAL — MORRISON MEDICAL, LTDMORRISON MEDICAL — MORRISON MEDICAL, LTD
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. |
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.