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STINGRAY SURGICAL PRODUCTS

US

Last updated September 17, 2026

Information

Country
US
Address
1701 Costa Del Sol, Boca Raton, FL, 33432
Website
—
LinkedIn
—
Facebook
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Email
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Phone
—
PRRC Contact
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EUDAMED SRN
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FDA FEI Number
3006059917
DUNS Number
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Catalogue (4782)

Page 71 of 96
DeviceModel / ReferenceRegistriesClassStatus
Stingray Surgical Products S03-699NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-268FGD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-678RSU30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-677TRU30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-180NSU345
FDA UDI
Class IIActive
Stingray Surgical Products S02-675TRS
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-230FGU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-678NSSU20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-651D30
FDA UDI
Class IIActive
Stingray Surgical Products S03-568NSU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-696TSD20
FDA UDI
Class IIActive
Stingray Surgical Products S02-676RSD45
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-675TRD45
FDA UDI
Class IIUnknown
Stingray Surgical Products G92-039
FDA UDI
Class IActive
Stingray Surgical Products S03-697NSSU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-677SD45
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-674TRD20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-681TU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-396
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-674RSD30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-469SPD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-862EF
FDA UDI
Class IIActive
Stingray Surgical Products S02-696RSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-653
FDA UDI
Class IIActive
Stingray Surgical Products S0325-282FGD15
FDA UDI
Class IIActive
Stingray Surgical Products S03-696SU30
FDA UDI
Class IIActive
Stingray Surgical Products S02-697SU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-675SU20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-458SPRD30
FDA UDI
Class IIActive
Stingray Surgical Products G64-040I
FDA UDI
Class IActive
Stingray Surgical Products S03-695NSU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-425R
FDA UDI
Class IIActive
Stingray Surgical Products S03-696NSRS
FDA UDI
Class IIActive
Stingray Surgical Products S03-678RSU20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-377
FDA UDI
Class IIActive
Stingray Surgical Products S03-681D45
FDA UDI
Class IIActive
Stingray Surgical Products S03-680TRSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-445NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-678TRSD30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-488NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-598NSD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-676D20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-465NSD45
FDA UDI
Class IIActive
Stingray Surgical Products S02-057
FDA UDI
Class IIActive
Stingray Surgical Products S03-685U20
FDA UDI
Class IIActive
Stingray Surgical Products S03-460SPU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-683RD45
FDA UDI
Class IIActive
Stingray Surgical Products G92-003
FDA UDI
Class IActive
Stingray Surgical Products S03-233FG
FDA UDI
Class IIActive
Stingray Surgical Products S02-680SD30
FDA UDI
Class IIActive

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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
May 23, 2012Z-2011-2012—terminated

On 05/23/2012, Stingray Surgical Products, LLC., Boca Raton, FL initiated a recall initiated due to "Instructions For Use" of Bipolar Forceps not being cleared by FDA and incorrect "Instructions For Use" . The sterilization instructions have been altered without the clearance of the FDA.