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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 6 of 96
DeviceModel / ReferenceRegistriesClassStatus
Stingray Surgical Products S02-685TRD20
FDA UDI
Class IIActive
Stingray Surgical Products S02-685D45
FDA UDI
Class IIActive
Stingray Surgical Products S03-674RSU45
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-364NSS
FDA UDI
Class IIActive
Stingray Surgical Products S03-130NSD30
FDA UDI
Class IIActive
Stingray Surgical Products G92-124
FDA UDI
Class IActive
Stingray Surgical Products S03-183NSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-695TU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-596NSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-674D45
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-681NSRSD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-469SPRU30
FDA UDI
Class IIActive
Stingray Surgical Products S02-696RSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-677RSD45
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-648TRD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-677RSD30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-390SPD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-683TRD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-674TRS
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-547NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-651TRSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-400S
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-450NSD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-652U45
FDA UDI
Class IIActive
Stingray Surgical Products S02-416
FDA UDI
Class IIActive
Stingray Surgical Products S03-697D20
FDA UDI
Class IIActive
Stingray Surgical Products S03-055T
FDA UDI
Class IIActive
Stingray Surgical Products S03-677SU30
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-698TRSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-268FGD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-681R
FDA UDI
Class IIActive
Stingray Surgical Products S03-543NSU30
FDA UDI
Class IIActive
Stingray Surgical Products S02-683SD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-648TRD45
FDA UDI
Class IIActive
Stingray Surgical Products S02-071T
FDA UDI
Class IIActive
Stingray Surgical Products S03-376
FDA UDI
Class IIActive
Stingray Surgical Products S03-695NSR
FDA UDI
Class IIActive
Stingray Surgical Products S03-263NSD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-699NSRSD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-683TRD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-094NSSS
FDA UDI
Class IIActive
Stingray Surgical Products S03-465SP
FDA UDI
Class IIActive
Stingray Surgical Products S03-403NS
FDA UDI
Class IIActive
Stingray Surgical Products S02-695RSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-695NSS
FDA UDI
Class IIActive
Stingray Surgical Products S03-548SPU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-303NS
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-677TSU30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-648NSR
FDA UDI
Class IIActive
Stingray Surgical Products S03-681U45
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.