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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 91 of 96
DeviceModel / ReferenceRegistriesClassStatus
Stingray Surgical Products S03-280FGD20
FDA UDI
Class IIActive
Stingray Surgical Products S02-412
FDA UDI
Class IIActive
Stingray Surgical Products S03-698NSSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-676NSRSD20
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-683TRAB
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-580NSU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-653TRU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-655SD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-414
FDA UDI
Class IIActive
Stingray Surgical Products S034-685NSS
FDA UDI
Class IIActive
Stingray Surgical Products S02-680RU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-565NSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-535NSRU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-681RU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-699TD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-463NSRD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-538NSR
FDA UDI
Class IIActive
Stingray Surgical Products S02-652TSU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-652TU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-651TRSU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-675TRSU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-652RU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-685NSSD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-057NSS
FDA UDI
Class IIActive
Stingray Surgical Products S02-695TU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-655TRSD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-652NSU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-674TRSU30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-427R
FDA UDI
Class IIActive
Stingray Surgical Products S02-086S
FDA UDI
Class IIActive
Stingray Surgical Products S03-697SU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-845EF
FDA UDI
Class IIActive
Stingray Surgical Products S03-683RSU45
FDA UDI
Class IIActive
Stingray Surgical Products G64-012I
FDA UDI
Class IActive
Stingray Surgical Products S03-491NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-402SPRD20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-697U20
FDA UDI
Class IIActive
Stingray Surgical Products G74-050I
FDA UDI
Class IActive
Stingray Surgical Products S03-235NSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-465SPRD30
FDA UDI
Class IIActive
Stingray Surgical Products S033-453NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-676NSS
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-683NSS
FDA UDI
Class IIActive
Stingray Surgical Products S02-695D20
FDA UDI
Class IIActive
Stingray Surgical Products S03-457SPRU30
FDA UDI
Class IIActive
Stingray Surgical Products G64-022I
FDA UDI
Class IActive
Stingray Surgical Products S03-567NSD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-678TRU45
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-410
FDA UDI
Class IIActive
Stingray Surgical Products S03-055NS
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.