Endo-Therapeutics, Inc.
Endo-Therapeutics, Inc. holds FDA 510(k) medical device clearances, first cleared 1993, most recent 2009, with 1 FDA device recall on record.
Top product codes for Endo-Therapeutics, Inc.
FDA recalls by Endo-Therapeutics, Inc.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Endo-Therapeutics, Inc.
- K090796 — MULTI-BITE HOT BIOPSY FORCEPS
- K031026 — ETI BIPOLAR HEMOSTATIC PROBE
- K023603 — ENDO-GLIDE GUIDEWIRE
- K012725 — TISSUE GRASPING FORCEPS, SCISSORS, CLAMPS AND DISSECTORS FOR LAPAROSCOPIC SURGERIES
- K012977 — VARICES INJECTION NEEDLE
- K926549 — ENDOCATH ELECTROPHYSIOLOGY CATHETER
- K925392 — BIOPSY FORCEPS
Data sourced from openFDA. This site is unofficial and independent of the FDA.