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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 14 of 96
DeviceModel / ReferenceRegistriesClassStatus
Stingray Surgical Products S02-682RD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-240FGU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-148NSU30
FDA UDI
Class IIActive
Stingray Surgical Products S02-696RS
FDA UDI
Class IIActive
Stingray Surgical Products S03-677TRD30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-450SPU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-676TRU30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-530NSR
FDA UDI
Class IIActive
Stingray Surgical Products S03-674TRS
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-685RU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-468SPRU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-304NS
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-699NSU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-414NSR
FDA UDI
Class IIActive
Stingray Surgical Products S03-651TRU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-698TRAB
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-655
FDA UDI
Class IIActive
Stingray Surgical Products S02-653RSU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-243FGD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-696SD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-450SPU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-396
FDA UDI
Class IIActive
Stingray Surgical Products S03-696TRU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-599NSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-530NSRU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-699D30
FDA UDI
Class IIActive
Stingray Surgical Products S03-113NSU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-653D30
FDA UDI
Class IIActive
Stingray Surgical Products S03-680SD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-651RD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-465NSU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-268NSU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-652RSU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-682TS
FDA UDI
Class IIActive
Stingray Surgical Products S03-697U30
FDA UDI
Class IIActive
Stingray Surgical Products S02-698U30
FDA UDI
Class IIActive
Stingray Surgical Products S03-384SER
FDA UDI
Class IIActive
Stingray Surgical Products S03-655TRD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-676SD30
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-696RD20
FDA UDI
Class IIActive
Stingray Surgical Products G64-008I
FDA UDI
Class IActive
Stingray Surgical Products S03-696RSU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-443R
FDA UDI
Class IIActive
Stingray Surgical Products S02-390R
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-418R
FDA UDI
Class IIActive
Stingray Surgical Products S03-057S
FDA UDI
Class IIActive
Stingray Surgical Products S03-539SPU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-458SPU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-678TD30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-677RSU20
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.