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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 87 of 96
DeviceModel / ReferenceRegistriesClassStatus
Stingray Surgical Products S03-568NSD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-681TSU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-396R
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-455NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-425
FDA UDI
Class IIActive
Stingray Surgical Products S02-372
FDA UDI
Class IIActive
Stingray Surgical Products S02-655TD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-168NSD20
FDA UDI
Class IIActive
Stingray Surgical Products G92-058
FDA UDI
Class IActive
Stingray Surgical Products S03-118NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-400SPRD30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-450SPD45
FDA UDI
Class IIActive
Stingray Surgical Products S02-651U30
FDA UDI
Class IIActive
Stingray Surgical Products S03-655NSRSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-590NSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-651NSD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-653TRD20
FDA UDI
Class IIActive
Stingray Surgical Products S02-652SU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-614T
FDA UDI
Class IIActive
Stingray Surgical Products S03-539SPRD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-641NS
FDA UDI
Class IIActive
Stingray Surgical Products S02-409R
FDA UDI
Class IIActive
Stingray Surgical Products S02-634TRS
FDA UDI
Class IIActive
Stingray Surgical Products S03-683NSU30
FDA UDI
Class IIActive
Stingray Surgical Products S02-685TSD45
FDA UDI
Class IIActive
Stingray Surgical Products S02-674TRD30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-467NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-655TRS
FDA UDI
Class IIActive
Stingray Surgical Products S02-682U45
FDA UDI
Class IIActive
Stingray Surgical Products S03-098NSSS
FDA UDI
Class IIActive
Stingray Surgical Products S03-110NSU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-071S
FDA UDI
Class IIActive
Stingray Surgical Products S02-695RU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-390
FDA UDI
Class IIActive
Stingray Surgical Products S02-641TS
FDA UDI
Class IIActive
Stingray Surgical Products S03-235NSU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-683NSSU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-683R
FDA UDI
Class IIActive
Stingray Surgical Products S03-675TD20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-117NSD20
FDA UDI
Class IIActive
Stingray Surgical Products S02-376
FDA UDI
Class IIActive
Stingray Surgical Products S03-068
FDA UDI
Class IIActive
Stingray Surgical Products S02-096
FDA UDI
Class IIActive
Stingray Surgical Products S03-459SPD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-682U30
FDA UDI
Class IIActive
Stingray Surgical Products S03-676TRU45
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-440NS
FDA UDI
Class IIActive
Stingray Surgical Products S02-676TRSU30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-676NSRSD45
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-677TRSD30
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.