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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 92 of 96
DeviceModel / ReferenceRegistriesClassStatus
Stingray Surgical Products S03-237FGD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-525NSHR
FDA UDI
Class IIActive
Stingray Surgical Products S03-431
FDA UDI
Class IIActive
Stingray Surgical Products S02-651D20
FDA UDI
Class IIActive
Stingray Surgical Products S03-394SPD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-459NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-695TU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-457SPRD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-545SP
FDA UDI
Class IIActive
Stingray Surgical Products S03-537NSRD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-674NSSU20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-238NSU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-682D45
FDA UDI
Class IIActive
Stingray Surgical Products S03-577NSD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-123NSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-681RSU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-677TRSU45
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-681SU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-655D45
FDA UDI
Class IIActive
Stingray Surgical Products S03-465SPR
FDA UDI
Class IIActive
Stingray Surgical Products S03-439
FDA UDI
Class IIActive
Stingray Surgical Products S02-629
FDA UDI
Class IIActive
Stingray Surgical Products S02-676U30
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-648D30
FDA UDI
Class IIActive
Stingray Surgical Products S03-160NSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-677NSRSD45
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-381NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-695TRU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-065NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-698NSSU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-682SU30
FDA UDI
Class IIActive
Stingray Surgical Products S02-410R
FDA UDI
Class IIActive
Stingray Surgical Products S03-675TRSD45
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-683NSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-539NSU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-453NSRU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-655D20
FDA UDI
Class IIActive
Stingray Surgical Products S03-547SPRD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-675R
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-414
FDA UDI
Class IIActive
Stingray Surgical Products S02-655SU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-675NSD30
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-683U30
FDA UDI
Class IIActive
Stingray Surgical Products S02-699RSD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-698TRD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-698SD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-653NSSU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-459SPD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-600
FDA UDI
Class IIActive
Stingray Surgical Products S03-678RSD45
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.