Standard Bariatrics is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Standard Bariatrics - FDA 510(k) Cleared Devices
Recent clearances: Standard Bougie, 38 Fr. and Hand Pump, Standard Bougie, 38 Fr., Titan SGS
10
Total
10
Cleared
0
Denied
Standard Bariatrics has 10 FDA 510(k) cleared general & plastic surgery devices. Based in Cincinnati, US.
Last cleared in 2021. Active since 2016.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Standard Bariatrics
10 devices
Cleared
Sep 23, 2021
Standard Bougie, 38 Fr. and Hand Pump
Gastroenterology & Urology
27d
Cleared
Jun 29, 2021
Standard Bougie, 38 Fr.
Gastroenterology & Urology
137d
Cleared
CT
Apr 28, 2021
Titan SGS
General & Plastic Surgery
86d
Cleared
Apr 09, 2020
Standard Trocar
General & Plastic Surgery
38d
Cleared
Apr 08, 2020
Standard Bougie
Gastroenterology & Urology
268d
Cleared
Apr 18, 2019
Disposable Standard Clamp
General & Plastic Surgery
22d
Cleared
Sep 27, 2018
Disposable Standard Clamp
General & Plastic Surgery
100d
Cleared
Jul 19, 2017
Disposable Standard Clamp
General & Plastic Surgery
162d
Cleared
Oct 24, 2016
Standard Clamp
General & Plastic Surgery
124d
Cleared
May 02, 2016
Standard Clamp
General & Plastic Surgery
164d