Medical Device Manufacturer · CA , Ontario K7s 1l8

Terray Manufacturing, Inc. - FDA 510(k) Cleared Devices

9 submissions · 8 cleared · Since 1987

Total

Cleared

Denied

Terray Manufacturing, Inc. has 8 FDA 510(k) cleared medical devices. Based in Ontario K7s 1l8, CA.

Historical record: 8 cleared submissions from 1987 to 1992. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Terray Manufacturing, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Terray Manufacturing, Inc.

9 devices

1-9 of 9

Cleared Feb 03, 1992

THORACIC ANTERIOR SPINAL FIXATION PLATE

K910874 · KWQ

Orthopedic · 339d

Cleared Oct 13, 1988

CASF CANCELLOUS BONE SCREW, BT650

K882934 · HWC

Orthopedic · 92d

Cleared Sep 23, 1988

CASF DRILL GUIDE DG 170

K882871 · LYQ

Orthopedic · 74d

Cleared Aug 10, 1988

CASF STERILIZATION TRAY

K883125 · FSM

General & Plastic Surgery · 15d

Cleared Aug 10, 1988

CASF STERILIZATION TRAY

K883193 · FSM

General & Plastic Surgery · 13d

Cleared Jun 30, 1987

ANTERIOR SPINAL FIXATION PLATE

RD 140 SURGICAL BENDER

K870084 · HXW

Orthopedic · 20d

Data Source

Sourced from the FDA 510(k) public files . 174,477 total devices indexed.

Last updated: Mar 22, 2026

Terray Manufacturing, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) cleared devices by Terray Manufacturing, Inc.

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