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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
—
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 79 of 96
DeviceModel / ReferenceRegistriesClassStatus
Stingray Surgical Products S03-533SP
FDA UDI
Class IIActive
Stingray Surgical Products S03-648NSU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-267NSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-377SER
FDA UDI
Class IIActive
Stingray Surgical Products S03-130NSD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-648NSU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-681D20
FDA UDI
Class IIActive
Stingray Surgical Products S03-699RSD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-463SPR
FDA UDI
Class IIActive
Stingray Surgical Products S03-453SPRU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-676TRSU20
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-680TS
FDA UDI
Class IIActive
Stingray Surgical Products S02-674TSD30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-698NSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-682TRSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-539SPRD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-469NSRD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-655TRSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-268NSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-676NSSD45
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-392SPRD45
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-651NSRSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-396NSRD30
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-681RSU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-651R
FDA UDI
Class IIActive
Stingray Surgical Products S03-392SPRD20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-457NSD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-681TRSU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-547SPU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-460SPRD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-543SPRD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-630NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-651RSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-402R
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-652TD20
FDA UDI
Class IIActive
Stingray Surgical Products S02-695TRD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-675NSS
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-653SU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-681TRSD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-636S
FDA UDI
Class IIActive
Stingray Surgical Products S03-267NS
FDA UDI
Class IIActive
Stingray Surgical Products G92-085
FDA UDI
Class IActive
Stingray Surgical Products S03-632SF
FDA UDI
Class IIActive
Stingray Surgical Products S03-368NSS
FDA UDI
Class IIActive
Stingray Surgical Products S03-680U30
FDA UDI
Class IIActive
Stingray Surgical Products S03-237NSD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-084NSS
FDA UDI
Class IIActive
Stingray Surgical Products S036-539NSR
FDA UDI
Class IIActive
Stingray Surgical Products S03-696TRS
FDA UDI
Class IIActive
Stingray Surgical Products S02-678S
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.