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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 4 of 96
DeviceModel / ReferenceRegistriesClassStatus
Stingray Surgical Products S03-533NSD20
FDA UDI
Class IIActive
Stingray Surgical Products S02-676RSD30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-467SPRU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-628
FDA UDI
Class IIActive
Stingray Surgical Products S03-457SP
FDA UDI
Class IIActive
Stingray Surgical Products S03-549NS
FDA UDI
Class IIActive
Stingray Surgical Products S02-674U45
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-575NSU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-641
FDA UDI
Class IIActive
Stingray Surgical Products S02-682RSU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-685NSRSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-698TS
FDA UDI
Class IIActive
Stingray Surgical Products S03-652RSD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-421
FDA UDI
Class IIActive
Stingray Surgical Products S03-465SPU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-681T
FDA UDI
Class IIActive
Stingray Surgical Products S03-455NSRD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-677NSSU45
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-396R
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-230FG
FDA UDI
Class IIActive
Stingray Surgical Products S03-678SU45
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-651T
FDA UDI
Class IIActive
Stingray Surgical Products S03-390NSR
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-123NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-698NSRSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-457NSU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-697RU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-685SD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-576NS
FDA UDI
Class IIActive
Stingray Surgical Products S02-651RU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-450NSD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-676
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-653TS
FDA UDI
Class IIActive
Stingray Surgical Products S02-054S
FDA UDI
Class IIActive
Stingray Surgical Products S02-699TS
FDA UDI
Class IIActive
Stingray Surgical Products S03-652D20
FDA UDI
Class IIActive
Stingray Surgical Products S03-685TRSD20
FDA UDI
Class IIActive
Stingray Surgical Products S02-698TR
FDA UDI
Class IIActive
Stingray Surgical Products S03-699SD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-537NSRU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-088NSS
FDA UDI
Class IIActive
Stingray Surgical Products S03-394SPRD20
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-685U30
FDA UDI
Class IIActive
Stingray Surgical Products S03-697TRSU30
FDA UDI
Class IIActive
Stingray Surgical Products S02-697TSD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-288NSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-450NSU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-676SU20
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-060S
FDA UDI
Class IIActive
Stingray Surgical Products S02-675SU30
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.