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.
FDA 510(k) cleared devices by Erbe USA, Inc.
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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