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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 74 of 96
DeviceModel / ReferenceRegistriesClassStatus
Stingray Surgical Products S02-405
FDA UDI
Class IIActive
Stingray Surgical Products S02-071
FDA UDI
Class IIActive
Stingray Surgical Products S03-533NSRU20
FDA UDI
Class IIActive
Stingray Surgical Products G92-013
FDA UDI
Class IActive
Stingray Surgical Products S03-523NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-676NSRSD30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-245FGZ
FDA UDI
Class IIActive
Stingray Surgical Products S03-674
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-652RS
FDA UDI
Class IIActive
Stingray Surgical Products S03-459NSRD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-699S
FDA UDI
Class IIActive
Stingray Surgical Products S02-652SD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-678NSRSU45
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-677NSR
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-699NSS
FDA UDI
Class IIActive
Stingray Surgical Products S03-652TRSD45
FDA UDI
Class IIActive
Stingray Surgical Products S02-067T
FDA UDI
Class IIActive
Stingray Surgical Products S02-685TSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-400SPR
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-089
FDA UDI
Class IIActive
Stingray Surgical Products S03-540NSU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-569NSU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-376NS
FDA UDI
Class IIActive
Stingray Surgical Products S02-675
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-685U20
FDA UDI
Class IIActive
Stingray Surgical Products S03-540NSU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-237FG
FDA UDI
Class IIActive
Stingray Surgical Products S04-800
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-655NSSD45
FDA UDI
Class IIActive
Stingray Surgical Products S02-064T
FDA UDI
Class IIActive
Stingray Surgical Products S03-080NSSS
FDA UDI
Class IIActive
Stingray Surgical Products S03-683D30
FDA UDI
Class IIActive
Stingray Surgical Products S03-539NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-377NS
FDA UDI
Class IIActive
Stingray Surgical Products S02-695SD20
FDA UDI
Class IIActive
Stingray Surgical Products S02-681RD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-682NSD45
FDA UDI
Class IIActive
Stingray Surgical Products S02-651TSD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-695TSD45
FDA UDI
Class IIActive
Stingray Surgical Products S02-695TRSU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-441NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-698TRSU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-697T
FDA UDI
Class IIActive
Stingray Surgical Products S03-696SU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-681SU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-581NSD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-651NSSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-243FGU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-680SU30
FDA UDI
Class IIActive
Stingray Surgical Products S02-698TD30
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.