FDA applicant
Sybron Corp.
FDA records 37 decisions for Sybron Corp. (Mchenry, IL) from 1977 to 1986: 37 510(k) clearances. Most are in product codes GEI (Electrosurgical, Cutting & Coagulation &…) and FRC (Indicator, Biological Sterilization Process). 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 Sybron Corp.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Sybron Corp. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Sybron Corp.’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 “Sybron”
FDA records each applicant name separately; these may or may not be the same firm.