E Surgical, LLC

FDA Regulatory Profile

E Surgical, LLC appears in FDA public data with 0 recalls, 5 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Feb 6, 2024.

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Known Names

E Surgical, E. Surgical

Recent 510(k) Clearances

K-NumberDeviceDate
K233115Hawkeye Control Unit with Eyas EndoscopeFeb 6, 2024
K231126Eblator DeviceAug 2, 2023
K071080ELECTROSURGICAL INFANT PATIENT RETURN ELECTRODE, DUAL PLATE WITH CORD, MODEL EP 211MAug 31, 2007
K061878ELECTRODE COATED BALL, MODEL AB302C; NEEDLE, MODEL AN301C; BLADE, MODEL AE301HCOct 24, 2006
K060255E SURGICAL ELECTROSURGICAL PATIENT RETURN ELECTRODE, DUAL PLATE WITH CORD AND ELECTROSURGICAL PATIENMar 31, 2006