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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 2 of 96
DeviceModel / ReferenceRegistriesClassStatus
Stingray Surgical Products S03-548SPRD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-450NSRD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-696NSR
FDA UDI
Class IIActive
Stingray Surgical Products S03-583NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-280NSU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-549NSRD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-468NSRD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-460SPRU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-695TRD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-459SPRU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-418NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-653TRU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-674SD45
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-230FGD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-547SPRU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-653U20
FDA UDI
Class IIActive
Stingray Surgical Products S02-675TU45
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-539NSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-683
FDA UDI
Class IIActive
Stingray Surgical Products S03-594NS
FDA UDI
Class IIActive
Stingray Surgical Products S02-681TU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-655RSD45
FDA UDI
Class IIActive
Stingray Surgical Products S02-640TRS
FDA UDI
Class IIActive
Stingray Surgical Products S03-651TU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-699TU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-394NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-374
FDA UDI
Class IIActive
Stingray Surgical Products S03-648SD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-548SPU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-641RS
FDA UDI
Class IIActive
Stingray Surgical Products S03-508NSHR
FDA UDI
Class IIActive
Stingray Surgical Products S03-280FGU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-368S
FDA UDI
Class IIActive
Stingray Surgical Products S03-533SPU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-678TRU20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-674TR
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-683TR
FDA UDI
Class IIActive
Stingray Surgical Products S02-685U45
FDA UDI
Class IIActive
Stingray Surgical Products S03-406R
FDA UDI
Class IIActive
Stingray Surgical Products S03-578NSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-469SPR
FDA UDI
Class IIActive
Stingray Surgical Products S02-685RSU30
FDA UDI
Class IIActive
Stingray Surgical Products S02-634
FDA UDI
Class IIActive
Stingray Surgical Products S03-677NSRSD20
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-653SD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-545SPR
FDA UDI
Class IIActive
Stingray Surgical Products S02-676T
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-457SPD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-233NSU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-675TRSU45
FDA UDI
Class IIUnknown

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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.