Allwin Medical Devices, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Allwin Medical Devices, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ARMADA Ureteral Dilator Set, ARMADA Nottingham One Step Dilator, ARMADA Amplatz Renal Dilator Sets, ARMADA Renal Dilator, Glider Amplatz Sheath, ARMADA Renal Dilator with Amplatz Sheath, Fascial Dilator Set, Introducer Sheath, Introducer Catheter, allFlex Ureteral Catheters, Krait Ureteral Catheters, SureStrip Vitrification Straw, SureLock Vitrification Straw
7
Total
6
Cleared
0
Denied
Allwin Medical Devices, Inc. has 6 FDA 510(k) cleared medical devices. Based in Anaheim, US.
Last cleared in 2023. Active since 2019. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Allwin Medical Devices, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Allwin Medical Devices, Inc.
7 devices
Cleared
May 05, 2023
ARMADA Ureteral Dilator Set, ARMADA Nottingham One Step Dilator, ARMADA...
Gastroenterology & Urology
414d
Cleared
Oct 13, 2022
allFlex Ureteral Catheters, Krait Ureteral Catheters
Gastroenterology & Urology
213d
Cleared
Jun 04, 2021
SureStrip Vitrification Straw, SureLock Vitrification Straw
Obstetrics & Gynecology
175d
Cleared
Jul 01, 2020
Allwin Embryo Transfer Catheters (ETC), Allwin ETC Stylets and Soft Obturators
Obstetrics & Gynecology
152d
Cleared
Dec 02, 2019
Ureteral Stent Open Tip/Closed Tip/Intraoperative Tip, Ureteral Stent via...
Gastroenterology & Urology
263d
Cleared
Nov 25, 2019
Allwin Ovum Pickup Needles (ACE Single Lumen Ovum Pickup Needle, OVUMPICK...
Obstetrics & Gynecology
263d
Cleared
Nov 14, 2019
Allwin Intra Uterine Insemination Catheters (INSEMINA and INSEMINA Open Tip...
Obstetrics & Gynecology
255d