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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
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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 1 of 96
DeviceModel / ReferenceRegistriesClassStatus
Stingray Surgical Products S02-622
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-699SU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-653TRU30
FDA UDI
Class IIActive
Stingray Surgical Products S02-651TRS
FDA UDI
Class IIActive
Stingray Surgical Products S03-235NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-537NSD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-390NSD45
FDA UDI
Class IIActive
Stingray Surgical Products S02-060TS
FDA UDI
Class IIActive
Stingray Surgical Products S03-697RSU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-092
FDA UDI
Class IIActive
Stingray Surgical Products S03-648TRSD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-463SPD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-457NSRD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-265NS
FDA UDI
Class IIActive
Stingray Surgical Products S02-655SU30
FDA UDI
Class IIActive
Stingray Surgical Products S02-698RSD45
FDA UDI
Class IIActive
Stingray Surgical Products S02-697TRD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-676R
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-465NSRU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-547NSR
FDA UDI
Class IIActive
Stingray Surgical Products S03-696RSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-651TRU30
FDA UDI
Class IIActive
Stingray Surgical Products S02-695TRSD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-681RD30
FDA UDI
Class IIActive
Stingray Surgical Products G03-212
FDA UDI
Class IActive
Stingray Surgical Products S03-652SU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-591NSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-120NSD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-640NSS
FDA UDI
Class IIActive
Stingray Surgical Products S03-245NSD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-425NSR
FDA UDI
Class IIActive
Stingray Surgical Products S02-634S
FDA UDI
Class IIActive
Stingray Surgical Products S03-599NSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-128NSU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-677RSU30
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-648TSD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-682TRSU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-697U20
FDA UDI
Class IIActive
Stingray Surgical Products S03-281NSD20
FDA UDI
Class IIActive
Stingray Surgical Products S02-677RSU20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-696TRSD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-598NSU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-676RSU20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-263FGD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-453NSRD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-674TRSD20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-676TRD20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-599NSD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-652TRSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-676RSU30
FDA UDI
Class IIUnknown

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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.