Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

STINGRAY SURGICAL PRODUCTS

US

Last updated September 17, 2026

Information

Country
US
Address
1701 Costa Del Sol, Boca Raton, FL, 33432
Website
—
LinkedIn
—
Facebook
—
Email
—
Phone
—
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
3006059917
DUNS Number
—

Catalogue (4782)

Page 84 of 96
DeviceModel / ReferenceRegistriesClassStatus
Stingray Surgical Products S03-681R
FDA UDI
Class IIActive
Stingray Surgical Products S02-680R
FDA UDI
Class IIActive
Stingray Surgical Products S03-676NSSU20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-597NSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-697NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-651TS
FDA UDI
Class IIActive
Stingray Surgical Products S03-634TR
FDA UDI
Class IIActive
Stingray Surgical Products S02-685D20
FDA UDI
Class IIActive
Stingray Surgical Products S03-683SU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-676SD45
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-676RS
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-233NSD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-447
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-064S
FDA UDI
Class IIActive
Stingray Surgical Products S02-699RU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-653D45
FDA UDI
Class IIActive
Stingray Surgical Products S03-651TRS
FDA UDI
Class IIActive
Stingray Surgical Products S02-082SS
FDA UDI
Class IIActive
Stingray Surgical Products S03-545NSR
FDA UDI
Class IIActive
Stingray Surgical Products S03-281FGD20
FDA UDI
Class IIActive
Stingray Surgical Products G50-035I
FDA UDI
Class IActive
Stingray Surgical Products S03-068NSS
FDA UDI
Class IIActive
Stingray Surgical Products S03-680TU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-683NSRSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-699TRU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-696TD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-648NSRSD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-651TU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-685
FDA UDI
Class IIActive
Stingray Surgical Products S03-465SPRU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-681TU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-677NSS
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-681NSSU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-535SPRD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-682TU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-545NSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-127NS
FDA UDI
Class IIActive
Stingray Surgical Products S02-648TRSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-674TRSD30
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-674RSD30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-655TU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-400SPD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-674NSRSU30
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-699SU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-678RU45
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-697D30
FDA UDI
Class IIActive
Stingray Surgical Products S02-675TD45
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-537NSU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-676TSU30
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-674TRU45
FDA UDI
Class IIUnknown

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

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.