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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 20 of 96
DeviceModel / ReferenceRegistriesClassStatus
Stingray Surgical Products S02-683RSU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-374S
FDA UDI
Class IIActive
Stingray Surgical Products S03-695TRSD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-678TRSD20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-547SPRU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-420NSR
FDA UDI
Class IIActive
Stingray Surgical Products S03-547NSRD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-469SPU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-538NSRU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-235FG
FDA UDI
Class IIActive
Stingray Surgical Products S03-457NSRD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-543NS
FDA UDI
Class IIActive
Stingray Surgical Products S02-677T
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-652SD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-113NSU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-390
FDA UDI
Class IIActive
Stingray Surgical Products S03-443
FDA UDI
Class IIActive
Stingray Surgical Products S03-453SPD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-677NSD20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-090NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-651NSSD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-455NSRU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-533NSRD45
FDA UDI
Class IIActive
Stingray Surgical Products S02-682TSU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-682TU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-653NS
FDA UDI
Class IIActive
Stingray Surgical Products S02-651
FDA UDI
Class IIActive
Stingray Surgical Products S03-390NSRD30
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-698TRSD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-680TSD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-675TRSD20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-143NSU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-675NSRSD45
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-678TRSU20
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-056
FDA UDI
Class IIActive
Stingray Surgical Products S02-695RSU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-680TRU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-682NSRS
FDA UDI
Class IIActive
Stingray Surgical Products S03-655SD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-682SU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-583NSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-168NSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-580NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-545SPRD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-457NSD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-394NSRD30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-066
FDA UDI
Class IIActive
Stingray Surgical Products S02-699RSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-683U30
FDA UDI
Class IIActive
Stingray Surgical Products S03-653SD30
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.