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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 86 of 96
DeviceModel / ReferenceRegistriesClassStatus
Stingray Surgical Products S03-677RSD30
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-677D45
FDA UDI
Class IIUnknown
Stingray Surgical Products S036-442NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-450NSRU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-448
FDA UDI
Class IIActive
Stingray Surgical Products S03-640R
FDA UDI
Class IIActive
Stingray Surgical Products S03-533SPU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-458NS
FDA UDI
Class IIActive
Stingray Surgical Products S02-655TRSU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-569NSU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-065S
FDA UDI
Class IIActive
Stingray Surgical Products S03-281NSD30
FDA UDI
Class IIActive
Stingray Surgical Products G92-023
FDA UDI
Class IActive
Stingray Surgical Products S02-648TSD20
FDA UDI
Class IIActive
Stingray Surgical Products S02-698TRD45
FDA UDI
Class IIActive
Stingray Surgical Products S02-358S
FDA UDI
Class IIActive
Stingray Surgical Products S03-468SPRD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-653TRD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-653NSRSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-402NSRD45
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-680TRSU30
FDA UDI
Class IIActive
Stingray Surgical Products S02-676SD30
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-655TRSU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-054S
FDA UDI
Class IIActive
Stingray Surgical Products S03-548NSRU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-648TU30
FDA UDI
Class IIActive
Stingray Surgical Products S02-653TR
FDA UDI
Class IIActive
Stingray Surgical Products S03-094NSS
FDA UDI
Class IIActive
Stingray Surgical Products S02-634TS
FDA UDI
Class IIActive
Stingray Surgical Products S02-678TU45
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-697RSD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-696TRD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-235FGD45
FDA UDI
Class IIActive
Stingray Surgical Products S02-675U20
FDA UDI
Class IIUnknown
Stingray Surgical Products G92-083
FDA UDI
Class IActive
Stingray Surgical Products S02-655RD45
FDA UDI
Class IIActive
Stingray Surgical Products S02-699RD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-697RSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-566NSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-681NSSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-682RS
FDA UDI
Class IIActive
Stingray Surgical Products S03-237NSD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-675TD30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-695SU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-235NSU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-680TD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-263FG
FDA UDI
Class IIActive
Stingray Surgical Products S03-678NSU20
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-683TRU30
FDA UDI
Class IIActive
Stingray Surgical Products S02-655D30
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.