FDA applicant
Anchor Products Co.
FDA records 7 decisions for Anchor Products Co. (Addison, IL) from 1979 to 2009: 7 510(k) clearances. Most are in product codes GCJ (Laparoscope, General & Plastic Surgery) and GES (Blade, Scalpel). 2 recalls are linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Anchor Products Co.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2009
2026 so far, outlined.
Recalls per year
2in 2010
Class I Class II/III not classified
Planning a device like Anchor Products 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 “Anchor”
FDA records each applicant name separately; these may or may not be the same firm.