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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
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LinkedIn
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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 88 of 96
DeviceModel / ReferenceRegistriesClassStatus
Stingray Surgical Products S03-458SPU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-540NSRD45
FDA UDI
Class IIActive
Stingray Surgical Products S02-683RD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-682TRSD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-652TRS
FDA UDI
Class IIActive
Stingray Surgical Products S03-683NSRS
FDA UDI
Class IIActive
Stingray Surgical Products S03-545SPD20
FDA UDI
Class IIActive
Stingray Surgical Products S02-648RS
FDA UDI
Class IIActive
Stingray Surgical Products S03-450SPD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-685NSSU30
FDA UDI
Class IIActive
Stingray Surgical Products G92-033
FDA UDI
Class IActive
Stingray Surgical Products S02-683RS
FDA UDI
Class IIActive
Stingray Surgical Products G03-310
FDA UDI
Class IActive
Stingray Surgical Products S03-652NSR
FDA UDI
Class IIActive
Stingray Surgical Products S03-655TRU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-238FG
FDA UDI
Class IIActive
Stingray Surgical Products S02-683TD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-435
FDA UDI
Class IIActive
Stingray Surgical Products S02-625
FDA UDI
Class IIActive
Stingray Surgical Products S03-548NSRU30
FDA UDI
Class IIActive
Stingray Surgical Products S02-682TD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-547SP
FDA UDI
Class IIActive
Stingray Surgical Products S02-648U30
FDA UDI
Class IIActive
Stingray Surgical Products S03-674NS
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-695SU30
FDA UDI
Class IIActive
Stingray Surgical Products S02-674D30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-140NSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-463NSRD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-096S
FDA UDI
Class IIActive
Stingray Surgical Products S02-676TSU45
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-641NSR
FDA UDI
Class IIActive
Stingray Surgical Products S02-696TSU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-683TS
FDA UDI
Class IIActive
Stingray Surgical Products S02-681RU30
FDA UDI
Class IIActive
Stingray Surgical Products S02-082
FDA UDI
Class IIActive
Stingray Surgical Products S03-069NSS
FDA UDI
Class IIActive
Stingray Surgical Products S03-247NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-465SPD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-674TU45
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-575NSU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-651TD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-683NS
FDA UDI
Class IIActive
Stingray Surgical Products S02-685TU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-698NSD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-286NSU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-545SPU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-530SPRU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-676NSSU45
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-530NSRD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-680RSU45
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.