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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
—
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 13 of 96
DeviceModel / ReferenceRegistriesClassStatus
Stingray Surgical Products S02-651SD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-535NSR
FDA UDI
Class IIActive
Stingray Surgical Products S02-695T
FDA UDI
Class IIActive
Stingray Surgical Products S03-402SPRD30
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-677U20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-685RSD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-676TS
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-400SPD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-288NSU30
FDA UDI
Class IIActive
Stingray Surgical Products S02-682SU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-333
FDA UDI
Class IIActive
Stingray Surgical Products S03-685TRD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-582NSU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-675D45
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-648NSRSU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-678RS
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-568NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-460NSRU20
FDA UDI
Class IIActive
Stingray Surgical Products G50-259I
FDA UDI
Class IActive
Stingray Surgical Products S02-675TRD20
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-678TRU20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-440NSR
FDA UDI
Class IIActive
Stingray Surgical Products S03-695SU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-699TU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-140NSD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-392NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-467SPD20
FDA UDI
Class IIActive
Stingray Surgical Products S02-682TSD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-677SU45
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-697TU30
FDA UDI
Class IIActive
Stingray Surgical Products S02-681RSD45
FDA UDI
Class IIActive
Stingray Surgical Products S02-360
FDA UDI
Class IIActive
Stingray Surgical Products S03-575NSD20
FDA UDI
Class IIActive
Stingray Surgical Products S02-682TSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-682TRSD20
FDA UDI
Class IIActive
Stingray Surgical Products S02-699
FDA UDI
Class IIActive
Stingray Surgical Products S03-545SPRU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-677TD20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-533NSRU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-539SPD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-453NSD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-678TRU30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-696TD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-675TRSU20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-549SPRD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-698TU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-699NSR
FDA UDI
Class IIActive
Stingray Surgical Products S03-455SP
FDA UDI
Class IIActive
Stingray Surgical Products S03-651
FDA UDI
Class IIActive
Stingray Surgical Products S03-237FGU45
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.