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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 5 of 96
DeviceModel / ReferenceRegistriesClassStatus
Stingray Surgical Products S03-463SPRU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-652TRS
FDA UDI
Class IIActive
Stingray Surgical Products S02-682TU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-696NSRSU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-080
FDA UDI
Class IIActive
Stingray Surgical Products S03-450SP
FDA UDI
Class IIActive
Stingray Surgical Products S03-263FGU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-168NSD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-655RU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-683SD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-696TRSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-584NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-685SU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-368NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-641T
FDA UDI
Class IIActive
Stingray Surgical Products S02-104SS
FDA UDI
Class IIActive
Stingray Surgical Products S03-648RS
FDA UDI
Class IIActive
Stingray Surgical Products S02-685TRD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-468SPD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-641R
FDA UDI
Class IIActive
Stingray Surgical Products S03-682RSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-648SD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-674RSU30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-697TRSD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-681TSD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-539NSD45
FDA UDI
Class IIActive
Stingray Surgical Products S02-680RSD45
FDA UDI
Class IIActive
Stingray Surgical Products S02-676U20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-655NSRSD45
FDA UDI
Class IIActive
Stingray Surgical Products S02-653R
FDA UDI
Class IIActive
Stingray Surgical Products S03-675TRU30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-459SPU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-676TRS
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-260NSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-539SPRU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-469NSRU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-678NSS
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-598NSU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-695RSU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-648SD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-535NSD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-330NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-376SER
FDA UDI
Class IIActive
Stingray Surgical Products S02-652R
FDA UDI
Class IIActive
Stingray Surgical Products S03-674RSD20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-596NSD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-364S
FDA UDI
Class IIActive
Stingray Surgical Products S02-698RU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-183NSU30
FDA UDI
Class IIActive
Stingray Surgical Products S02-697U30
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.