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14 devices found
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Manufacturer: Puregraft, LLC
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Device · Manufacturer · Authorizations
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Status
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Registry
Class
Puregraft MicroFat Transfer Kit (19G) 50/MICRO19
Puregraft, LLC
·
,
United States
(FDA 510(k) applicant)
Not classified
GUDID
not on market
Withdrawn
GUDID
—
Puregraft 850
UDI-DI 10860407002222
Puregraft, LLC
·
,
United States
(FDA 510(k) applicant)
Class II
GUDID
not on market
Withdrawn
GUDID
II
2 variants
Puregraft 850
850/PURE
Withdrawn
Dermapose Refresh Syringe Stand
Puregraft, LLC
·
,
United States
(FDA 510(k) applicant)
Class I
GUDID
not on market
Withdrawn
GUDID
I
AutoPose Restore ABS-101035-1
Puregraft, LLC
·
,
United States
(FDA 510(k) applicant)
Class II
GUDID
not on market
Withdrawn
GUDID
II
Puregraft MicroFat Transfer Kit (21G) 50/MICRO21
Puregraft, LLC
·
,
United States
(FDA 510(k) applicant)
Not classified
GUDID
not on market
Withdrawn
GUDID
—
Puregraft 250
UDI-DI 20863445000301
Puregraft, LLC
·
,
United States
(FDA 510(k) applicant)
Class II
GUDID
not on market
Withdrawn
GUDID
II
2 variants
Puregraft 250
250/PURE
Withdrawn
Puregraft MicroFat Transfer Kit 50/MICRO
Puregraft, LLC
·
,
United States
(FDA 510(k) applicant)
Not classified
GUDID
not on market
Withdrawn
GUDID
—
Dermapose Access
Puregraft, LLC
·
,
United States
(FDA 510(k) applicant)
Class II
GUDID
not on market
Withdrawn
GUDID
II
Dermapose Refresh
Puregraft, LLC
·
,
United States
(FDA 510(k) applicant)
Class II
GUDID
not on market
Withdrawn
GUDID
II
Puregraft 50
Puregraft, LLC
·
,
United States
(FDA 510(k) applicant)
Class II
GUDID
not on market
Withdrawn
GUDID
II
Dermapose Access
Puregraft, LLC
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K200168
Active
Cleared 22 Apr 2020
Active
510(k)
510(k)
II
Dermapose Refresh
Puregraft, LLC
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K193363
Active
Cleared 14 Apr 2020
Active
510(k)
510(k)
II
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