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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
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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 78 of 96
DeviceModel / ReferenceRegistriesClassStatus
Stingray Surgical Products S03-104NSS
FDA UDI
Class IIActive
Stingray Surgical Products S02-697SU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-549SPRD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-698NSR
FDA UDI
Class IIActive
Stingray Surgical Products S03-698TD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-392S
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-676TRD45
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-699TD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-581NSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-396NSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-094NS
FDA UDI
Class IIActive
Stingray Surgical Products S02-640RS
FDA UDI
Class IIActive
Stingray Surgical Products S03-591NSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-545NSU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-576NSU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-655SD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-453SPU30
FDA UDI
Class IIActive
Stingray Surgical Products S02-439R
FDA UDI
Class IIActive
Stingray Surgical Products S02-696TSU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-160NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-539NSD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-636NSR
FDA UDI
Class IIActive
Stingray Surgical Products S02-098SS
FDA UDI
Class IIActive
Stingray Surgical Products S03-447NSR
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-685D30
FDA UDI
Class IIActive
Stingray Surgical Products S02-685TD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-062S
FDA UDI
Class IIActive
Stingray Surgical Products S02-696RU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-140NSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-080NSS
FDA UDI
Class IIActive
Stingray Surgical Products S03-286FGD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-237NSU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-676U30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-698NSRSU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-396SPRD45
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-459NSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-676NSR
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-439
FDA UDI
Class IIActive
Stingray Surgical Products S03-582NS
FDA UDI
Class IIActive
Stingray Surgical Products S02-084
FDA UDI
Class IIActive
Stingray Surgical Products S02-655TU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-674U30
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-429
FDA UDI
Class IIActive
Stingray Surgical Products S02-652U45
FDA UDI
Class IIActive
Stingray Surgical Products S03-521NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-593NSD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-547SPD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-648TRSU30
FDA UDI
Class IIActive
Stingray Surgical Products S02-698TRU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-681TRU20
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.