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 80 of 96
DeviceModel / ReferenceRegistriesClassStatus
Stingray Surgical Products S03-458NSD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-465SPU30
FDA UDI
Class IIActive
Stingray Surgical Products S02-699D30
FDA UDI
Class IIActive
Stingray Surgical Products S03-530SPRD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-677TRSU30
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-699RS
FDA UDI
Class IIActive
Stingray Surgical Products S02-068S
FDA UDI
Class IIActive
Stingray Surgical Products S03-265FGD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-180NSD45
FDA UDI
Class IIActive
Stingray Surgical Products S02-652TRSD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-300
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-697TRS
FDA UDI
Class IIActive
Stingray Surgical Products S03-676NSD45
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-685TU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-538NSU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-533NSR
FDA UDI
Class IIActive
Stingray Surgical Products S03-113NSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-699NSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-460NSRD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-460NSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-678NS
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-652NSRSD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-651TRSD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-549SPD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-699NSRSU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-678TD20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-530SPRU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-674NSU45
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-648TSU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-648RSD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-675TRD30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-547SPU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-675SD30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-118NSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-653TRU45
FDA UDI
Class IIActive
Stingray Surgical Products S02-680TSD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-538SP
FDA UDI
Class IIActive
Stingray Surgical Products S03-467NSRU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-655NSSU30
FDA UDI
Class IIActive
Stingray Surgical Products S02-098
FDA UDI
Class IIActive
Stingray Surgical Products S02-697TRSD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-653TRS
FDA UDI
Class IIActive
Stingray Surgical Products S03-071
FDA UDI
Class IIActive
Stingray Surgical Products S03-084
FDA UDI
Class IIActive
Stingray Surgical Products S03-086NSS
FDA UDI
Class IIActive
Stingray Surgical Products S02-699TD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-281FGU30
FDA UDI
Class IIActive
Stingray Surgical Products S02-699TSD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-090S
FDA UDI
Class IIActive
Stingray Surgical Products S01-080
FDA UDI
Class IActive

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.