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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 95 of 96
DeviceModel / ReferenceRegistriesClassStatus
Stingray Surgical Products S03-468SPR
FDA UDI
Class IIActive
Stingray Surgical Products S02-680RSU30
FDA UDI
Class IIActive
Stingray Surgical Products S02-438R
FDA UDI
Class IIActive
Stingray Surgical Products S03-090NSS
FDA UDI
Class IIActive
Stingray Surgical Products S03-280FGU30
FDA UDI
Class IIActive
Stingray Surgical Products S02-648RU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-545NSRD30
FDA UDI
Class IIActive
Stingray Surgical Products S036-538NSR
FDA UDI
Class IIActive
Stingray Surgical Products S03-235FGU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-281FGD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-102S
FDA UDI
Class IIActive
Stingray Surgical Products S02-681TRD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-247FGU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-695NSD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-080S
FDA UDI
Class IIActive
Stingray Surgical Products S03-469NSRU45
FDA UDI
Class IIActive
Stingray Surgical Products G74-045I
FDA UDI
Class IActive
Stingray Surgical Products S03-384
FDA UDI
Class IIActive
Stingray Surgical Products S02-655
FDA UDI
Class IIActive
Stingray Surgical Products S03-402SPRD45
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-652TRSD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-685RSU30
FDA UDI
Class IIActive
Stingray Surgical Products S02-678RSU20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-240NSU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-651TRSD30
FDA UDI
Class IIActive
Stingray Surgical Products G50-258I
FDA UDI
Class IActive
Stingray Surgical Products S03-396NSR
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-682RSD20
FDA UDI
Class IIActive
Stingray Surgical Products S02-681TR
FDA UDI
Class IIActive
Stingray Surgical Products S02-675SU45
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-685TRSD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-696NSRSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-233NSU30
FDA UDI
Class IIActive
Stingray Surgical Products S02-655TD20
FDA UDI
Class IIActive
Stingray Surgical Products S02-652TU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-539NSRD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-458NSRD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-683U20
FDA UDI
Class IIActive
Stingray Surgical Products S03-455NSRU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-651RSU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-676T
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-567NSU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-457NSRU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-458NSR
FDA UDI
Class IIActive
Stingray Surgical Products S03-682NSRSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-448R
FDA UDI
Class IIActive
Stingray Surgical Products S03-634NS
FDA UDI
Class IIActive
Stingray Surgical Products S02-371
FDA UDI
Class IIActive
Stingray Surgical Products S03-655D20
FDA UDI
Class IIActive
Stingray Surgical Products S02-648RD30
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.