FDA applicant
Disco-O-Tech Medical Technologies, Ltd.
FDA records 9 decisions for Disco-O-Tech Medical Technologies, Ltd. (Herzlia, IL) from 1999 to 2003: 9 510(k) clearances. Most are in product codes HSB (Rod, Fixation, Intramedullary And Accessories) and JDS (Nail, Fixation, Bone). Its devices cite 47 predicates, 20 of them its own earlier devices. 1 recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Disco-O-Tech Medical Technologies, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Disco-O-Tech Medical Technologies, Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Disco-O-Tech Medical Technologies, Ltd.’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 “Disco-O-Tech”
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