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MAST BIOSURGERY USA INC.

US

Last updated September 17, 2026

Information

Country
US
Address
6749 Top Gun St Ste 108, SAN DIEGO, CA, 92121
Website
—
LinkedIn
—
Facebook
—
Email
—
Phone
—
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
3004661493
DUNS Number
—

Catalogue (29)

DeviceModel / ReferenceRegistriesClassStatus
CardioWrap 100 x 130 x 0.05mm
FDA UDI
Class IIActive
SurgiWrap 100 x 130 x 0.05mm
FDA UDI
Class IIActive
SurgiWrap 130 x 200 x 0.02mm
FDA UDI
Class IIActive
SurgiWrap 130 x 200 x 0.05mm
FDA UDI
Class IIActive
SurgiWrap® 100 x 130 x 0.02mm
FDA UDI
Class IIUnknown
SurgiWrap® 180 x 280 x 0.05mm
FDA UDI
Class IIUnknown
SurgiWrap FROST 100 x 130 x 0.02mm
FDA UDI
Class IIActive
SurgiWrap® 180 x 280 x 0.02mm
FDA UDI
Class IIUnknown
SurgiWrap® 130 x 200 x 0.02mm
FDA UDI
Class IIUnknown
SurgiWrap® 100 x 130 x 0.05mm
FDA UDI
Class IIUnknown
CardioWrap® 130 x 200 x 0.05mm
FDA UDI
Class IIUnknown
CardioWrap® 100 x 130 x 0.02mm
FDA UDI
Class IIUnknown
OrthoWrap® 50 x 70 x 0.02mm
FDA UDI
Class IIUnknown
CardioWrap® 130 x 200 x 0.02mm
FDA UDI
Class IIUnknown
SurgiWrap FROST 50 x 65 x 0.02mm
FDA UDI
Class IIActive
SurgiWrap® 50 x 70 x 0.05mm
FDA UDI
Class IIUnknown
OrthoWrap 50mm x 70mm x 0.05mm
FDA UDI
Class IIActive
OrthoWrap 50mm x 70mm x 0.02mm
FDA UDI
Class IIActive
SurgiWrap® 130 x 200 x 0.05mm
FDA UDI
Class IIUnknown
SurgiWrap 100 x 130 x 0.02mm
FDA UDI
Class IIActive
CardioWrap 130 x 200 x 0.05mm
FDA UDI
Class IIActive
SurgiWrap FROST 130 x 200 x 0.02mm
FDA UDI
Class IIActive
SurgiWrap® 50 x 70 x 0.02mm
FDA UDI
Class IIUnknown
OrthoWrap® 50 x 70 x 0.05mm
FDA UDI
Class IIUnknown
CardioWrap® 100 x 130 x 0.05mm
FDA UDI
Class IIUnknown
Surgi-Wrap Mast Bioresorbable Sheet K050332
FDA 510(k)
Class IIActive
Surgi-Wrap Mast Tendon Sheet K063648
FDA 510(k)
Class IIActive
Cardio-Wrap K090637
FDA 510(k)
Class IIActive
Surgi-Wrap Mast Bioresorbable Sheet K061473
FDA 510(k)
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Recalls (1)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

DateRecall No.ClassStatusReason
Aug 26, 2014Z-1076-2015—terminated

The expiration date of the bar code on the envelope label did not match the expiration date next to the hourglass. The printed expiration date was August of 2017, while the bar code date read as July 31, 2017. The correct expiration date was July 31, 2017.