Erbe USA, Inc. - FDA 510(k) Cleared Devices
39
Total
39
Cleared
0
Denied
Erbe USA, Inc. has 39 FDA 510(k) cleared medical devices. Based in Lawrenceville, US.
Last cleared in 2022. Active since 1994. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Erbe USA, Inc. Filter by specialty or product code using the sidebar.
39 devices
Cleared
Aug 11, 2022
Erbe's Tubing/Cap Sets
Gastroenterology & Urology
108d
Cleared
Jun 27, 2019
ERBEFLO 2 Endo Quick Connect Pentax Scope Port Connector
Gastroenterology & Urology
28d
Cleared
May 23, 2019
ERBEFLO 2 Disposable Tubing System
Gastroenterology & Urology
86d
Cleared
Nov 06, 2018
ERBEFLO Olympus Scope Port Connector
Gastroenterology & Urology
60d
Cleared
Aug 31, 2016
Erbe’s CO2 Tubing/Cap Sets
Gastroenterology & Urology
29d
Cleared
Oct 27, 2015
ERBE WaterJet Model ERBEJET® 2 System with HybridAPC Probe
General & Plastic Surgery
343d
Cleared
May 04, 2015
ERBECRYO 2 Cryosurgical Unit with accessories
General & Plastic Surgery
14d
Cleared
Dec 18, 2014
Endo Quickconnect Olympus Scope Port Connector, Endo Quickconnect Pentax...
Gastroenterology & Urology
43d
Cleared
Dec 17, 2013
ERBEFLO CLEVERCAP HYBRID TUBING/CAP SET FOR PENTAX SCOPES, ERBEFLO CLEVERCAP...
Gastroenterology & Urology
144d
Cleared
Dec 11, 2013
ERBE ESU MODEL VIO DV WITH ACCESSORIES
General & Plastic Surgery
55d
Cleared
Mar 22, 2011
ERBEFLO CLEVERCAP HYBRID TUBING/CAP SETS FOR OLYMPUS MODELS 160 AND 180...
Gastroenterology & Urology
95d
Cleared
Dec 23, 2010
ERBEFLO 2 DISPOSABLE TUBING SYSTEM
Gastroenterology & Urology
51d
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