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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 72 of 96
DeviceModel / ReferenceRegistriesClassStatus
Stingray Surgical Products S03-695TRSD20
FDA UDI
Class IIActive
Stingray Surgical Products S02-681U30
FDA UDI
Class IIActive
Stingray Surgical Products S02-648TRU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-652TRSU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-682D30
FDA UDI
Class IIActive
Stingray Surgical Products S03-400NSRD45
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-655SU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-245FGD45
FDA UDI
Class IIActive
Stingray Surgical Products S02-696TS
FDA UDI
Class IIActive
Stingray Surgical Products S03-685NSU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-187NSU30
FDA UDI
Class IIActive
Stingray Surgical Products G92-027
FDA UDI
Class IActive
Stingray Surgical Products S02-697U45
FDA UDI
Class IIActive
Stingray Surgical Products S03-240NSU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-653SU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-372NSS
FDA UDI
Class IIActive
Stingray Surgical Products S02-695TU30
FDA UDI
Class IIActive
Stingray Surgical Products S02-648TSU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-680RD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-548SPRD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-230NSD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-088NSSS
FDA UDI
Class IIActive
Stingray Surgical Products S02-652TS
FDA UDI
Class IIActive
Stingray Surgical Products S03-286NSD20
FDA UDI
Class IIActive
Stingray Surgical Products S02-392
FDA UDI
Class IIActive
Stingray Surgical Products S02-371S
FDA UDI
Class IIActive
Stingray Surgical Products S03-248FGD45
FDA UDI
Class IIActive
Stingray Surgical Products S02-678TS
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-682NSSU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-681TD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-683TD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-680NSSU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-056TS
FDA UDI
Class IIActive
Stingray Surgical Products S03-465SPD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-469SPD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-696TRU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-683RSD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-469SP
FDA UDI
Class IIActive
Stingray Surgical Products S03-681TRSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-247NSU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-288NSD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-675U30
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-440R
FDA UDI
Class IIActive
Stingray Surgical Products S03-653TU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-681TU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-653
FDA UDI
Class IIActive
Stingray Surgical Products S03-396SP
FDA UDI
Class IIActive
Stingray Surgical Products S02-698U20
FDA UDI
Class IIActive
Stingray Surgical Products S03-503NSHR
FDA UDI
Class IIActive
Stingray Surgical Products S03-674D30
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.