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12 devices found
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Manufacturer: Zipline Medical, Inc.
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Device · Manufacturer · Authorizations
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Registry
Class
Zip 24 Surgical Skin Closure Device 667616001
Zipline Medical, Inc.
·
,
FDA registration: United States
Class I
GUDID
not on market
Withdrawn
GUDID
I
Zip 16 Surgical Skin Closure Device PS1160
Zipline Medical, Inc.
·
,
FDA registration: United States
Class I
GUDID
not on market
Withdrawn
GUDID
I
Zip 4 Surgical Skin Closure Device 667613001
Zipline Medical, Inc.
·
,
FDA registration: United States
Class I
GUDID
not on market
Withdrawn
GUDID
I
Zip 24 Surgical Skin Closure Device 900024001
Zipline Medical, Inc.
·
,
FDA registration: United States
Class I
GUDID
not on market
Withdrawn
GUDID
I
Zip 8i Surgical Skin Closure Device 900008001
Zipline Medical, Inc.
·
,
FDA registration: United States
Class I
GUDID
not on market
Withdrawn
GUDID
I
Zip 16 Surgical Skin Closure Device 900016001
Zipline Medical, Inc.
·
,
FDA registration: United States
Class I
GUDID
not on market
Withdrawn
GUDID
I
Zip 24 Surgical Skin Closure Device PS1240
Zipline Medical, Inc.
·
,
FDA registration: United States
Class I
GUDID
not on market
Withdrawn
GUDID
I
Zip 4 Surgical Skin Closure Device PS2040
Zipline Medical, Inc.
·
,
FDA registration: United States
Class I
GUDID
not on market
Withdrawn
GUDID
I
Zip 4 Surgical Skin Closure Device 900004001
Zipline Medical, Inc.
·
,
FDA registration: United States
Class I
GUDID
not on market
Withdrawn
GUDID
I
Zip 16 Surgical Skin Closure Device 667615001
Zipline Medical, Inc.
·
,
FDA registration: United States
Class I
GUDID
not on market
Withdrawn
GUDID
I
Zip 8i Surgical Skin Closure Device 667614001
Zipline Medical, Inc.
·
,
FDA registration: United States
Class I
GUDID
not on market
Withdrawn
GUDID
I
Zip 4 Skin Closure Device
Zipline Medical, Inc.
·
,
FDA registration: United States
Class I
FDA 510(k)
K170003
Active
Cleared 18 Aug 2017
Active
510(k)
510(k)
I
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