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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 82 of 96
DeviceModel / ReferenceRegistriesClassStatus
Stingray Surgical Products S02-675RSD20
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-674TRD20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-681TRSD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-677NSSD30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-677NSD30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-685NSS
FDA UDI
Class IIActive
Stingray Surgical Products S02-695TRS
FDA UDI
Class IIActive
Stingray Surgical Products S02-677RD45
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-675NSRSU20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-676TR
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-652NSRS
FDA UDI
Class IIActive
Stingray Surgical Products S03-577NS
FDA UDI
Class IIActive
Stingray Surgical Products S02-674TD45
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-457SPRU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-685
FDA UDI
Class IIActive
Stingray Surgical Products S03-699TRSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-676SD20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-677U20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-675RSU30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-680RSD45
FDA UDI
Class IIActive
Stingray Surgical Products S02-676TU30
FDA UDI
Class IIUnknown
Stingray Surgical Products G50-265I
FDA UDI
Class IActive
Stingray Surgical Products S02-055S
FDA UDI
Class IIActive
Stingray Surgical Products S03-104SS
FDA UDI
Class IIActive
Stingray Surgical Products S03-678TRSU45
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-648NSSU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-481NSHR
FDA UDI
Class IIActive
Stingray Surgical Products S02-674RSD20
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-067TS
FDA UDI
Class IIActive
Stingray Surgical Products G50-261I
FDA UDI
Class IActive
Stingray Surgical Products S03-675TR
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-374NS
FDA UDI
Class IIActive
Stingray Surgical Products S02-632
FDA UDI
Class IIActive
Stingray Surgical Products S03-538SPR
FDA UDI
Class IIActive
Stingray Surgical Products S03-591NSD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-243FG
FDA UDI
Class IIActive
Stingray Surgical Products S03-160NSU30
FDA UDI
Class IIActive
Stingray Surgical Products S02-680TD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-698RSU30
FDA UDI
Class IIActive
Stingray Surgical Products S02-651TRD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-648NSSD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-699TSU20
FDA UDI
Class IIActive
Stingray Surgical Products G03-204
FDA UDI
Class IActive
Stingray Surgical Products S03-683TRSD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-698TD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-868EF
FDA UDI
Class IIActive
Stingray Surgical Products S03-545SPU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-390SPR
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-358
FDA UDI
Class IIActive
Stingray Surgical Products S03-678TRS
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.