FDA applicant
Greenfield Medical Technologies, Inc.
FDA records 1 decision for Greenfield Medical Technologies, Inc. (Northborough, MA) in 1999: 1 510(k) clearance. All are in product code MGP (Dressing, Wound And Burn, Occlusive). 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 Greenfield Medical Technologies, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Greenfield Medical Technologies, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Greenfield Medical Technologies, Inc.’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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