FDA applicant
Grieshaber & Co.
FDA records 15 decisions for Grieshaber & Co. (Langhorne, PA) from 1986 to 1995: 15 510(k) clearances. Most are in product codes EQH (Source, Carrier, Fiberoptic Light) and HQE (Instrument, Vitreous Aspiration And Cutting…). No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Grieshaber & Co.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Grieshaber & Co. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Grieshaber & Co.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
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