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 15 of 96
DeviceModel / ReferenceRegistriesClassStatus
Stingray Surgical Products S03-676TRU20
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-697TU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-392SP
FDA UDI
Class IIActive
Stingray Surgical Products S03-652TU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-680TU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-483NSHR
FDA UDI
Class IIActive
Stingray Surgical Products S02-655TU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-677D30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-402SPD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-674D20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-538SPRU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-458NSRU30
FDA UDI
Class IIActive
Stingray Surgical Products G03-118
FDA UDI
Class IActive
Stingray Surgical Products S03-592NSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-458NSRD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-680TU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-653TU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-685TRSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-530NSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-698D45
FDA UDI
Class IIActive
Stingray Surgical Products S03-380NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-678NSD30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-675RSD20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-675NSD20
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-674RU30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-453NSRD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-427NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-685S
FDA UDI
Class IIActive
Stingray Surgical Products S03-247FGU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-625
FDA UDI
Class IIActive
Stingray Surgical Products S03-460NSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-655NSSD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-652NSSD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-245FGU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-630SF
FDA UDI
Class IIActive
Stingray Surgical Products S03-429
FDA UDI
Class IIActive
Stingray Surgical Products G03-210
FDA UDI
Class IActive
Stingray Surgical Products S02-699TU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-653SD45
FDA UDI
Class IIActive
Stingray Surgical Products S02-695TRSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-441NSR
FDA UDI
Class IIActive
Stingray Surgical Products S03-676TRU30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-651RSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-547SPU30
FDA UDI
Class IIActive
Stingray Surgical Products S02-652TU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-362
FDA UDI
Class IIActive
Stingray Surgical Products S02-675RU20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-455SPD20
FDA UDI
Class IIActive
Stingray Surgical Products S02-640TS
FDA UDI
Class IIActive
Stingray Surgical Products S02-681SU20
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.