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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
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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 73 of 96
DeviceModel / ReferenceRegistriesClassStatus
Stingray Surgical Products S02-696TRSD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-267FGU30
FDA UDI
Class IIActive
Stingray Surgical Products S02-676TD20
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-412R
FDA UDI
Class IIActive
Stingray Surgical Products S03-677TU20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-063T
FDA UDI
Class IIActive
Stingray Surgical Products S02-685RSD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-071NSS
FDA UDI
Class IIActive
Stingray Surgical Products S03-674NSS
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-394SPR
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-655TRU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-188NSD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-438NS
FDA UDI
Class IIActive
Stingray Surgical Products S02-653RSU30
FDA UDI
Class IIActive
Stingray Surgical Products S02-652TRU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-443RSS
FDA UDI
Class IIActive
Stingray Surgical Products S03-457NSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-655TRSD45
FDA UDI
Class IIActive
Stingray Surgical Products S02-682D20
FDA UDI
Class IIActive
Stingray Surgical Products S03-458NSU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-680NSSD45
FDA UDI
Class IIActive
Stingray Surgical Products S02-682RD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-543NSD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-233NSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-634NSS
FDA UDI
Class IIActive
Stingray Surgical Products S02-683TRSD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-698TSU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-390R
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-533SPD20
FDA UDI
Class IIActive
Stingray Surgical Products S02-697RSU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-599NS
FDA UDI
Class IIActive
Stingray Surgical Products S02-088S
FDA UDI
Class IIActive
Stingray Surgical Products S03-068T
FDA UDI
Class IIActive
Stingray Surgical Products S03-235NSD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-120NSU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-653U20
FDA UDI
Class IIActive
Stingray Surgical Products S03-551NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-695U45
FDA UDI
Class IIActive
Stingray Surgical Products S03-537SPD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-655NSU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-685TRSD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-648R
FDA UDI
Class IIActive
Stingray Surgical Products S03-695U20
FDA UDI
Class IIActive
Stingray Surgical Products S03-652U30
FDA UDI
Class IIActive
Stingray Surgical Products S03-458SPD45
FDA UDI
Class IIActive
Stingray Surgical Products G03-236
FDA UDI
Class IActive
Stingray Surgical Products S02-676TSD45
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-648TRSD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-247NSU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-065T
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.