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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 11 of 96
DeviceModel / ReferenceRegistriesClassStatus
Stingray Surgical Products S03-503NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-288NSU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-675TRSU30
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-698U45
FDA UDI
Class IIActive
Stingray Surgical Products S02-653RU30
FDA UDI
Class IIActive
Stingray Surgical Products S02-699RU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-580NSU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-584NSD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-549NSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-460SP
FDA UDI
Class IIActive
Stingray Surgical Products S03-680NSD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-683NSRSD45
FDA UDI
Class IIActive
Stingray Surgical Products G92-106
FDA UDI
Class IActive
Stingray Surgical Products S03-584NSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-543NSD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-681
FDA UDI
Class IIActive
Stingray Surgical Products S03-548NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-699TRSU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-680TRD45
FDA UDI
Class IIActive
Stingray Surgical Products S02-697RSU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-096S
FDA UDI
Class IIActive
Stingray Surgical Products S02-653RD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-406R
FDA UDI
Class IIActive
Stingray Surgical Products S02-653TRD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-400NSD20
FDA UDI
Class IIActive
Stingray Surgical Products S02-652RD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-163NSU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-685NSSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-695TRSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-653NSRSD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-675SD45
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-530NSRU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-655TSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-245FGU45Z
FDA UDI
Class IIActive
Stingray Surgical Products S03-265FGU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-676NSRSU45
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-467SPU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-698NSSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-653D30
FDA UDI
Class IIActive
Stingray Surgical Products S02-680RS
FDA UDI
Class IIActive
Stingray Surgical Products S03-677TRU20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-263FGD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-089NSS
FDA UDI
Class IIActive
Stingray Surgical Products S03-457NSRU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-695S
FDA UDI
Class IIActive
Stingray Surgical Products S03-285NSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-286NSU30
FDA UDI
Class IIActive
Stingray Surgical Products S02-651TSU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-674NSRSU45
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-678NSSD20
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.