Medical Device Manufacturer · US , Natick , MA

Endo Technic Corp. - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 1986

Total

Cleared

Denied

Endo Technic Corp. has 10 FDA 510(k) cleared medical devices. Based in Natick, US.

Historical record: 10 cleared submissions from 1986 to 1999.

Browse the FDA 510(k) cleared devices submitted by Endo Technic Corp. Filter by specialty or product code using the sidebar.

Endo Technic Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Endo Technic Corp.

10 devices

1-10 of 10

General & Plastic Surgery · 88d

Cleared Aug 24, 1994

LAPAROSCOPIC INST. (SCISSORS,FORCEPS,NEEDLEHOLDER)

K925079 · HET

Obstetrics & Gynecology · 686d

Cleared Mar 09, 1994

LAPAROSCOPIC IRRIGATION/ASPIRATION HANDPIECE

K930756 · HET

Obstetrics & Gynecology · 390d

Cleared Feb 28, 1994

LAPAROSCOPIC INSTRUMENTS

K925114 · HFI

Obstetrics & Gynecology · 507d

Cleared Mar 30, 1993

TROCAR

K924058 · GCJ

General & Plastic Surgery · 230d

General & Plastic Surgery · 114d

Cleared Feb 27, 1987

SOLUSET CALCIUM DEMINERALIZING SOLUTION

K864976 · EKS

Dental · 70d

Cleared Jul 22, 1986

SET CANAL SEALER PASTE

K862129 · EKM

Dental · 48d

Endo Technic Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Endo Technic Corp.

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