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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 12 of 96
DeviceModel / ReferenceRegistriesClassStatus
Stingray Surgical Products S02-695TSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-648TR
FDA UDI
Class IIActive
Stingray Surgical Products S02-676TR
FDA UDI
Class IIUnknown
Stingray Surgical Products G50-263I
FDA UDI
Class IActive
Stingray Surgical Products S03-655NS
FDA UDI
Class IIActive
Stingray Surgical Products S02-682SU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-652NSRSD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-697SD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-652NSSD45
FDA UDI
Class IIActive
Stingray Surgical Products S02-678U20
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-677TRU20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-468NSR
FDA UDI
Class IIActive
Stingray Surgical Products G03-318
FDA UDI
Class IActive
Stingray Surgical Products S031-636NS
FDA UDI
Class IIActive
Stingray Surgical Products S02-678TD45
FDA UDI
Class IIUnknown
Stingray Surgical Products G50-260I
FDA UDI
Class IActive
Stingray Surgical Products S02-698S
FDA UDI
Class IIActive
Stingray Surgical Products S02-683RU30
FDA UDI
Class IIActive
Stingray Surgical Products S02-423
FDA UDI
Class IIActive
Stingray Surgical Products S02-651RD45
FDA UDI
Class IIActive
Stingray Surgical Products S02-653TD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-281NSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-640TRS
FDA UDI
Class IIActive
Stingray Surgical Products S03-697TD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-681
FDA UDI
Class IIActive
Stingray Surgical Products S03-449NS
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-676TRD30
FDA UDI
Class IIUnknown
Stingray Surgical Products G92-020
FDA UDI
Class IActive
Stingray Surgical Products S03-677RSD20
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-067S
FDA UDI
Class IIActive
Stingray Surgical Products S03-612T
FDA UDI
Class IIActive
Stingray Surgical Products S02-680TRSU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-680SD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-653NSSD45
FDA UDI
Class IIActive
Stingray Surgical Products S02-685SU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-677RU20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-578NS
FDA UDI
Class IIActive
Stingray Surgical Products S02-380SER
FDA UDI
Class IIActive
Stingray Surgical Products S02-676RU30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-699NSSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-653RSD20
FDA UDI
Class IIActive
Stingray Surgical Products S02-683SU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-685SD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-459NSR
FDA UDI
Class IIActive
Stingray Surgical Products S03-698TU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-593NSU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-651NSSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-680T
FDA UDI
Class IIActive
Stingray Surgical Products S02-651TU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-678D45
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.