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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 7 of 96
DeviceModel / ReferenceRegistriesClassStatus
Stingray Surgical Products S03-676U20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-653NSRSU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-682NSSD20
FDA UDI
Class IIActive
Stingray Surgical Products S02-696T
FDA UDI
Class IIActive
Stingray Surgical Products S03-682SD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-094SS
FDA UDI
Class IIActive
Stingray Surgical Products S02-682TRD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-683RD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-481NS
FDA UDI
Class IIActive
Stingray Surgical Products G64-019I
FDA UDI
Class IActive
Stingray Surgical Products S03-655RSD20
FDA UDI
Class IIActive
Stingray Surgical Products S02-683RSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-268NSD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-457NSRU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-651TRSD20
FDA UDI
Class IIActive
Stingray Surgical Products S02-674TRSU45
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-699TRD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-463NSR
FDA UDI
Class IIActive
Stingray Surgical Products G03-226
FDA UDI
Class IActive
Stingray Surgical Products S03-549NSU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-678D45
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-453NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-288FGD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-695D45
FDA UDI
Class IIActive
Stingray Surgical Products S02-680RSD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-698RSU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-631T
FDA UDI
Class IIActive
Stingray Surgical Products S03-655NSD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-651TRD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-549NSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-538SPU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-681SD45
FDA UDI
Class IIActive
Stingray Surgical Products S02-682SD3045
FDA UDI
Class IIActive
Stingray Surgical Products S02-653TRSD20
FDA UDI
Class IIActive
Stingray Surgical Products S02-680TU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-683T
FDA UDI
Class IIActive
Stingray Surgical Products S03-463SPD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-423NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-651NSD45
FDA UDI
Class IIActive
Stingray Surgical Products S02-630T
FDA UDI
Class IIActive
Stingray Surgical Products S03-648TRSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-653NSSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-548SPR
FDA UDI
Class IIActive
Stingray Surgical Products S034-538NSR
FDA UDI
Class IIActive
Stingray Surgical Products S03-055
FDA UDI
Class IIActive
Stingray Surgical Products S02-652SD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-447R
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-652TRU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-268NSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-682NSR
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.