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EUDAMED
22
FDA 510(k)
44
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1
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134
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17
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179
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11
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29
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23
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124
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184 devices found
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Device · Manufacturer · Authorizations
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Status
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Registry
Class
Nuda (Currently Called Ultra Sensitive)
Ansell, Inc.
·
,
FDA registration: United States
Class II
FDA 510(k)
K901111
Active
Cleared 27 Mar 1990
Active
510(k)
510(k)
II
Everlife Interferential Current Therapy, Model If-100507
Everlife Medical Equipment Co., Ltd.
·
,
Taiwan
(FDA 510(k) applicant)
Class II
FDA 510(k)
K070890
Active
Cleared 29 Jun 2007
Active
510(k)
510(k)
II
AutoCare
Micro Current Technology, Inc.
·
,
United States
Class IIa
CE/MDR
1000196662
Active
Valid to Jun 2031
FDA 510(k)
K032653
Active
Active
CE MDR
510(k)
EUDAMED
IIa
~[24~R Direct Current Bone Growth Stimulator
Zimmer, Inc.
·
,
United States
Class III
FDA PMA
P790008
Active
Approved 3 May 1982
Active
PMA
PMA
III
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Showing 181-184 of 184