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76 devices found
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sorted by relevance
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Manufacturer: Exsomed Corporation
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Device · Manufacturer · Authorizations
Verified
Status
Regime
Registry
Class
ArcPhix System EXARC903028
Exsomed Corporation
·
,
United States
(FDA 510(k) applicant)
Class II
GUDID
not on market
Withdrawn
GUDID
II
InFrame Implant EXINF922034
Exsomed Corporation
·
,
United States
(FDA 510(k) applicant)
Class II
GUDID
not on market
Withdrawn
GUDID
II
InFrame Implant EXINF922024
Exsomed Corporation
·
,
United States
(FDA 510(k) applicant)
Class II
GUDID
not on market
Withdrawn
GUDID
II
NanoPhix Implant EXINN921514
Exsomed Corporation
·
,
United States
(FDA 510(k) applicant)
Class II
GUDID
not on market
Withdrawn
GUDID
II
NanoPhix Implant EXINN921526
Exsomed Corporation
·
,
United States
(FDA 510(k) applicant)
Class II
GUDID
not on market
Withdrawn
GUDID
II
InFrame Implant EXINF922010
Exsomed Corporation
·
,
United States
(FDA 510(k) applicant)
Class II
GUDID
not on market
Withdrawn
GUDID
II
INnate Implant EXINN923635
Exsomed Corporation
·
,
United States
(FDA 510(k) applicant)
Class II
GUDID
not on market
Withdrawn
GUDID
II
NanoPhix Implant EXINN921507
Exsomed Corporation
·
,
United States
(FDA 510(k) applicant)
Class II
GUDID
not on market
Withdrawn
GUDID
II
ITN Implant EXITN924545
Exsomed Corporation
·
,
United States
(FDA 510(k) applicant)
Class II
GUDID
not on market
Withdrawn
GUDID
II
INnate Implant EXINN924555
Exsomed Corporation
·
,
United States
(FDA 510(k) applicant)
Class II
GUDID
not on market
Withdrawn
GUDID
II
INnate Implant EXINN923650
Exsomed Corporation
·
,
United States
(FDA 510(k) applicant)
Class II
GUDID
not on market
Withdrawn
GUDID
II
NanoPhix Implant EXINN921519
Exsomed Corporation
·
,
United States
(FDA 510(k) applicant)
Class II
GUDID
not on market
Withdrawn
GUDID
II
InFrame™ Cannulated Fixation System
Exsomed Corp.
·
,
FDA registration: United States
Class II
FDA 510(k)
K201430
Active
Cleared 20 Jun 2020
Active
510(k)
510(k)
II
ExsoMed INnate NanoTM Lag Screw System
Exsomed Corp.
·
,
FDA registration: United States
Class II
FDA 510(k)
K220892
Active
Cleared 27 Apr 2022
Active
510(k)
510(k)
II
Exsomed Wrist Plating System
Exsomed Corporation
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K192473
Active
Cleared 3 Dec 2019
Active
510(k)
510(k)
II
INnate Cannulated Screw System
Exsomed Corporation
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K183603
Active
Cleared 12 Mar 2019
Active
510(k)
510(k)
II
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Showing 61-76 of 76