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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 17 of 96
DeviceModel / ReferenceRegistriesClassStatus
Stingray Surgical Products S03-653SU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-696NSRSD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-676RU20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-632
FDA UDI
Class IIActive
Stingray Surgical Products S02-069
FDA UDI
Class IIActive
Stingray Surgical Products S03-634NSRS
FDA UDI
Class IIActive
Stingray Surgical Products S03-652R
FDA UDI
Class IIActive
Stingray Surgical Products S03-364S
FDA UDI
Class IIActive
Stingray Surgical Products S03-288FG
FDA UDI
Class IIActive
Stingray Surgical Products S03-460NSRD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-055TS
FDA UDI
Class IIActive
Stingray Surgical Products S03-675NSU30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-582NSD45
FDA UDI
Class IIActive
Stingray Surgical Products S02-641RS
FDA UDI
Class IIActive
Stingray Surgical Products S02-677
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-148NSU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-080
FDA UDI
Class IIActive
Stingray Surgical Products S03-543SPRD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-695TSU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-678RSD45
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-681TD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-651NSRSD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-697TRD20
FDA UDI
Class IIActive
Stingray Surgical Products S02-652D20
FDA UDI
Class IIActive
Stingray Surgical Products S03-652TRU30
FDA UDI
Class IIActive
Stingray Surgical Products S02-681RSU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-676NSRSU20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-110NSD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-459NSU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-468NSD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-530SPD20
FDA UDI
Class IIActive
Stingray Surgical Products G92-021
FDA UDI
Class IActive
Stingray Surgical Products S03-548NSRD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-057TS
FDA UDI
Class IIActive
Stingray Surgical Products S02-651TR
FDA UDI
Class IIActive
Stingray Surgical Products S03-465NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-143NSD45
FDA UDI
Class IIActive
Stingray Surgical Products S02-682TRS
FDA UDI
Class IIActive
Stingray Surgical Products S02-685RSD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-163NSD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-549NSRU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-653SD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-696NSU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-655TRD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-578NSD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-421
FDA UDI
Class IIActive
Stingray Surgical Products S03-685NSRSD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-675RSU45
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-403R
FDA UDI
Class IIActive
Stingray Surgical Products S02-431R
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.