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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 77 of 96
DeviceModel / ReferenceRegistriesClassStatus
Stingray Surgical Products S02-685TRU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-535SPD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-648NSSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-548SPRU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-678TSD30
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-677RSD45
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-653TRSU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-530SPD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-678D20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-699U30
FDA UDI
Class IIActive
Stingray Surgical Products S03-696TD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-238FGU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-678D30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-400SPRD45
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-084SS
FDA UDI
Class IIActive
Stingray Surgical Products S02-699TRSD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-543NSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-683NSSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-680TRSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-640RS
FDA UDI
Class IIActive
Stingray Surgical Products S03-651TU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-138NSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-237NSU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-653TRD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-439NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-590NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-640TR
FDA UDI
Class IIActive
Stingray Surgical Products S03-403
FDA UDI
Class IIActive
Stingray Surgical Products S02-431
FDA UDI
Class IIActive
Stingray Surgical Products S03-465NSU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-653RSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-548SPU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-655TRD20
FDA UDI
Class IIActive
Stingray Surgical Products S02-652TRSU30
FDA UDI
Class IIActive
Stingray Surgical Products S035-414NS
FDA UDI
Class IIActive
Stingray Surgical Products S02-094
FDA UDI
Class IIActive
Stingray Surgical Products S02-652TSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-133NSU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-695TR
FDA UDI
Class IIActive
Stingray Surgical Products S03-634R
FDA UDI
Class IIActive
Stingray Surgical Products S03-392NSRD30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-455NSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-061NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-187NSD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-420NS
FDA UDI
Class IIActive
Stingray Surgical Products G74-049I
FDA UDI
Class IActive
Stingray Surgical Products S02-699U20
FDA UDI
Class IIActive
Stingray Surgical Products S02-685TRD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-380
FDA UDI
Class IIActive
Stingray Surgical Products S03-674SU20
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.