Ethicon Endo-Surgery, Inc.
Ethicon Endo-Surgery, Inc. holds FDA 510(k) medical device clearances, first cleared 1992, most recent 2014, with 54 FDA device recalls on record.
Clearances by Ethicon Endo-Surgery, Inc. — page 2
101–112 of 112- K941027 — ENDOPATH OPTICAL OBTURATOR AND SLEEVE
- K942450 — ENDOPATH
- K940967 — MODIFIED ENDOPATH ILS
- K935756 — ENDOSCOPIC ARTICULATING MULTI-FEED STAPLER WITH RELOAD UNIT
- K932434 — PROXIMATE ARTICULATING LINEAR STAPLER
- K932476 — PROXIMATE RELOADABLE ARTICULATING LINEAR STAPLER
- K933160 — PROCEDURE KITS
- K924916 — ENDOPATH ENDOSCOPIC TISSUE RETRACTOR
- K931111 — ENDOPATH DISPOSABLE FLEXIBLE SURGICAL CANNULA
- K932282 — ENDOPATH II DISPOSABLE SURGICAL TROCAR & SLEEVE
- K924035 — ENDOPATH II DISPOSABLE SURGICAL TROCAR & SLEEVE
- K923679 — ENDOPATH TISSUE RETAINING COMPONENT
Data sourced from openFDA. This site is unofficial and independent of the FDA.