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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 19 of 96
DeviceModel / ReferenceRegistriesClassStatus
Stingray Surgical Products S03-453SPRU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-243FGU30
FDA UDI
Class IIActive
Stingray Surgical Products S02-651TD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-549SPRU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-445R
FDA UDI
Class IIActive
Stingray Surgical Products S03-535NSU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-699TRD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-566NSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-260FGD45
FDA UDI
Class IIActive
Stingray Surgical Products S02-061
FDA UDI
Class IIActive
Stingray Surgical Products S02-655TSU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-491NSHR
FDA UDI
Class IIActive
Stingray Surgical Products S02-695RU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-699RSD45
FDA UDI
Class IIActive
Stingray Surgical Products G74-040I
FDA UDI
Class IActive
Stingray Surgical Products S03-682TRD20
FDA UDI
Class IIActive
Stingray Surgical Products S02-655T
FDA UDI
Class IIActive
Stingray Surgical Products S02-057TS
FDA UDI
Class IIActive
Stingray Surgical Products S02-678TRSU45
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-651TRD45
FDA UDI
Class IIActive
Stingray Surgical Products S02-699TRD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-698SD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-595NSU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-460SPR
FDA UDI
Class IIActive
Stingray Surgical Products S02-448R
FDA UDI
Class IIActive
Stingray Surgical Products S03-288NSD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-653TSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-230NSU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-652TD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-680SD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-538SPU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-652SD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-648S
FDA UDI
Class IIActive
Stingray Surgical Products S03-468SP
FDA UDI
Class IIActive
Stingray Surgical Products S03-695SD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-465NSRD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-651TU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-118NSU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-682RS
FDA UDI
Class IIActive
Stingray Surgical Products S03-655T
FDA UDI
Class IIActive
Stingray Surgical Products S03-652TRSD20
FDA UDI
Class IIActive
Stingray Surgical Products S02-680TRSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-469SPU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-695TD45
FDA UDI
Class IIActive
Stingray Surgical Products S02-685RD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-675TD20
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-648TD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-530NSD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-685TSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-683TRSU30
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.