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 93 of 96
DeviceModel / ReferenceRegistriesClassStatus
Stingray Surgical Products S03-651D20
FDA UDI
Class IIActive
Stingray Surgical Products S03-392NSR
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-374NSS
FDA UDI
Class IIActive
Stingray Surgical Products S03-400
FDA UDI
Class IIActive
Stingray Surgical Products S03-238NSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-652S
FDA UDI
Class IIActive
Stingray Surgical Products S02-695TRD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-676TRS
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-140NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-674TD45
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-332NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-698SU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-263NSD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-677SD30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-695RSD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-674TS
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-678NSD45
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-597NSD45
FDA UDI
Class IIActive
Stingray Surgical Products S02-675TS
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-068T
FDA UDI
Class IIActive
Stingray Surgical Products S03-540NSD45
FDA UDI
Class IIActive
Stingray Surgical Products S02-676D45
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-683SD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-459SPRD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-655RSU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-648TRS
FDA UDI
Class IIActive
Stingray Surgical Products S03-260FGU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-675NSSD20
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-695TU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-468SPU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-697TRS
FDA UDI
Class IIActive
Stingray Surgical Products S03-539SPRD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-280NSD20
FDA UDI
Class IIActive
Stingray Surgical Products S02-677TRU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-442
FDA UDI
Class IIActive
Stingray Surgical Products S03-685NSSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-549SP
FDA UDI
Class IIActive
Stingray Surgical Products S03-652SU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-455SPRD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-681RS
FDA UDI
Class IIActive
Stingray Surgical Products S03-453SP
FDA UDI
Class IIActive
Stingray Surgical Products S03-539SPD20
FDA UDI
Class IIActive
Stingray Surgical Products S02-648SU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-636NSS
FDA UDI
Class IIActive
Stingray Surgical Products S02-695SD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-655RU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-545SPU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-062NSS
FDA UDI
Class IIActive
Stingray Surgical Products S02-425
FDA UDI
Class IIActive
Stingray Surgical Products S03-565NSD30
FDA UDI
Class IIActive

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.