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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 81 of 96
DeviceModel / ReferenceRegistriesClassStatus
Stingray Surgical Products S03-653R
FDA UDI
Class IIActive
Stingray Surgical Products S02-699D20
FDA UDI
Class IIActive
Stingray Surgical Products S02-063
FDA UDI
Class IIActive
Stingray Surgical Products S03-535SPU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-545SPRU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-230NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-685TRS
FDA UDI
Class IIActive
Stingray Surgical Products S03-288FGU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-696NSSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-460NSRD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-676NSSD20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-696TU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-678SU20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-410
FDA UDI
Class IIActive
Stingray Surgical Products S03-463SPU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-653NSU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-248NSU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-675TR
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-674TD20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-695D20
FDA UDI
Class IIActive
Stingray Surgical Products S03-455SPRU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-683TRU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-675TRU20
FDA UDI
Class IIUnknown
Stingray Surgical Products G92-005
FDA UDI
Class IActive
Stingray Surgical Products S03-458SPR
FDA UDI
Class IIActive
Stingray Surgical Products S03-233NSU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-674TD20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-127NSD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-137NSU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-082
FDA UDI
Class IIActive
Stingray Surgical Products S03-396SPD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-699SD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-508NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-130NSU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-678SD45
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-653NSU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-683TRSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-089NSSS
FDA UDI
Class IIActive
Stingray Surgical Products S03-535SPRU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-458NSU30
FDA UDI
Class IIActive
Stingray Surgical Products S02-683TRSD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-652RSU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-636T
FDA UDI
Class IIActive
Stingray Surgical Products S03-698NSSU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-685TSU30
FDA UDI
Class IIActive
Stingray Surgical Products S02-683TRU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-697RSU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-683TRU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-458SPRU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-533SPU30
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.