FDA applicant
Sherwood Medical Co.
FDA records 191 decisions for Sherwood Medical Co. (Mchenry, IL) from 1976 to 1998: 191 510(k) clearances. Most are in product codes FMF (Syringe, Piston) and FMI (Needle, Hypodermic, Single Lumen). Its devices cite 9 predicates, 2 of them its own earlier devices. 36 recalls are linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Sherwood Medical Co.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Sherwood Medical Co. since 2007.
Recalls per year
1in 2026
Class I Class II/III not classified
Planning a device like Sherwood Medical Co.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) ReportOther applicant names beginning “Sherwood”
FDA records each applicant name separately; these may or may not be the same firm.