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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 75 of 96
DeviceModel / ReferenceRegistriesClassStatus
Stingray Surgical Products S03-533NSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-648TS
FDA UDI
Class IIActive
Stingray Surgical Products S02-674TRSD30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-682NSU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-137NSD45
FDA UDI
Class IIActive
Stingray Surgical Products S02-675RSU30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-681SD45
FDA UDI
Class IIActive
Stingray Surgical Products S02-696TRU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-655TU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-118NSD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-247NSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-655SU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-655RSD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-245FG
FDA UDI
Class IIActive
Stingray Surgical Products S02-696U20
FDA UDI
Class IIActive
Stingray Surgical Products S03-651TRD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-699TS
FDA UDI
Class IIActive
Stingray Surgical Products S03-187NSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-390SPRD30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-458NSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-680SU30
FDA UDI
Class IIActive
Stingray Surgical Products S02-674RU20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-675TRSU20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-678RSD30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-183NSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-592NSU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-592NSU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-696NSD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-268NSU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-695TS
FDA UDI
Class IIActive
Stingray Surgical Products S02-678TSU30
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-652TU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-652NSD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-674S
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-674TRSU30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-581NSU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-675NSRSD20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-682RSD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-396SPD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-680NSU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-677TD30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-263NSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-540NSRU45
FDA UDI
Class IIActive
Stingray Surgical Products G92-028
FDA UDI
Class IActive
Stingray Surgical Products G92-123
FDA UDI
Class IActive
Stingray Surgical Products S03-674TRD30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-063S
FDA UDI
Class IIActive
Stingray Surgical Products S03-636TR
FDA UDI
Class IIActive
Stingray Surgical Products S03-653TS
FDA UDI
Class IIActive
Stingray Surgical Products S03-682NSRSU20
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.