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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 3 of 96
DeviceModel / ReferenceRegistriesClassStatus
Stingray Surgical Products S02-055
FDA UDI
Class IIActive
Stingray Surgical Products S03-138NSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-696D30
FDA UDI
Class IIActive
Stingray Surgical Products S03-685NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-676RSD20
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-698SU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-055S
FDA UDI
Class IIActive
Stingray Surgical Products S03-468NSRU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-543NSR
FDA UDI
Class IIActive
Stingray Surgical Products S03-696RSD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-865EF
FDA UDI
Class IIActive
Stingray Surgical Products S03-265NSD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-056NSS
FDA UDI
Class IIActive
Stingray Surgical Products S03-435R
FDA UDI
Class IIActive
Stingray Surgical Products S02-094S
FDA UDI
Class IIActive
Stingray Surgical Products S02-696TD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-677NSSU20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-675NS
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-467SPRD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-450NSRD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-267FGD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-469NSRU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-265FGD20
FDA UDI
Class IIActive
Stingray Surgical Products S02-680TSU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-062TS
FDA UDI
Class IIActive
Stingray Surgical Products S03-443NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-681NSU45
FDA UDI
Class IIActive
Stingray Surgical Products G03-306
FDA UDI
Class IActive
Stingray Surgical Products S03-685TRSU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-371
FDA UDI
Class IIActive
Stingray Surgical Products S03-681NSSD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-683NSR
FDA UDI
Class IIActive
Stingray Surgical Products S03-651NSRSU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-696TRSU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-674U20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-695R
FDA UDI
Class IIActive
Stingray Surgical Products S03-455SPRU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-681SD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-683TRSD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-358NSS
FDA UDI
Class IIActive
Stingray Surgical Products S02-681U20
FDA UDI
Class IIActive
Stingray Surgical Products S03-652RSD20
FDA UDI
Class IIActive
Stingray Surgical Products S02-680RSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-240FGU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-651NSSU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-685TU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-595NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-674NSSU45
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-674SU45
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-651TRSU45
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.