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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 8 of 96
DeviceModel / ReferenceRegistriesClassStatus
Stingray Surgical Products S02-651TRSU20
FDA UDI
Class IIActive
Stingray Surgical Products G03-316
FDA UDI
Class IActive
Stingray Surgical Products S03-697RSD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-652TD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-680TRSU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-088SS
FDA UDI
Class IIActive
Stingray Surgical Products S03-677TRSU20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-392NSRD20
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-648TRSD45
FDA UDI
Class IIActive
Stingray Surgical Products S02-674TRU30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-674NSD45
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-652
FDA UDI
Class IIActive
Stingray Surgical Products S02-674TRU20
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-648T
FDA UDI
Class IIActive
Stingray Surgical Products G03-312
FDA UDI
Class IActive
Stingray Surgical Products S03-651RS
FDA UDI
Class IIActive
Stingray Surgical Products S03-394NSRD20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-678SD45
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-696R
FDA UDI
Class IIActive
Stingray Surgical Products S03-681D30
FDA UDI
Class IIActive
Stingray Surgical Products S03-392NSD45
FDA UDI
Class IIActive
Stingray Surgical Products S02-680D20
FDA UDI
Class IIActive
Stingray Surgical Products S03-685NSRSU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-280FG
FDA UDI
Class IIActive
Stingray Surgical Products S02-697TSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-683TRSU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-677TRSD20
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-653TSU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-698TSD20
FDA UDI
Class IIActive
Stingray Surgical Products S02-697TD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-535SPRU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-697TU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-450NSRD45
FDA UDI
Class IIActive
Stingray Surgical Products G92-064
FDA UDI
Class IActive
Stingray Surgical Products S02-698TU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-651TSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-372S
FDA UDI
Class IIActive
Stingray Surgical Products S02-651T
FDA UDI
Class IIActive
Stingray Surgical Products S03-463NSD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-535NSRD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-538SPRD45
FDA UDI
Class IIActive
Stingray Surgical Products S02-697TS
FDA UDI
Class IIActive
Stingray Surgical Products S02-636S
FDA UDI
Class IIActive
Stingray Surgical Products S02-651RSU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-066NSS
FDA UDI
Class IIActive
Stingray Surgical Products S03-127NSD45
FDA UDI
Class IIActive
Stingray Surgical Products G92-105
FDA UDI
Class IActive
Stingray Surgical Products S03-695NSU45
FDA UDI
Class IIActive
Stingray Surgical Products G42-480I
FDA UDI
Class IActive
Stingray Surgical Products S03-547NSRU30
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.