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 9 of 96
DeviceModel / ReferenceRegistriesClassStatus
Stingray Surgical Products S03-655NSS
FDA UDI
Class IIActive
Stingray Surgical Products S02-682SD20
FDA UDI
Class IIActive
Stingray Surgical Products S02-674RSU45
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-696RSU30
FDA UDI
Class IIActive
Stingray Surgical Products S02-677TSU20
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-640S
FDA UDI
Class IIActive
Stingray Surgical Products G03-304
FDA UDI
Class IActive
Stingray Surgical Products S03-382SER
FDA UDI
Class IIActive
Stingray Surgical Products S03-678NSSD30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-655NSRSU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-089SS
FDA UDI
Class IIActive
Stingray Surgical Products S02-384SER
FDA UDI
Class IIActive
Stingray Surgical Products S02-447R
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-678TRU45
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-699NSSU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-071T
FDA UDI
Class IIActive
Stingray Surgical Products S03-699RSU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-648RSD45
FDA UDI
Class IIActive
Stingray Surgical Products S02-677U30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-698U20
FDA UDI
Class IIActive
Stingray Surgical Products S02-683
FDA UDI
Class IIActive
Stingray Surgical Products S02-695TD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-675TRU45
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-676TSD30
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-674TSD20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-695TRU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-370S
FDA UDI
Class IIActive
Stingray Surgical Products S02-414R
FDA UDI
Class IIActive
Stingray Surgical Products S02-685RSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-540SPD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-697TU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-697NSRSD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-595NSD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-468SPD20
FDA UDI
Class IIActive
Stingray Surgical Products S02-685RU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-648SU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-549SPRU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-680SU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-501NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-652NSD20
FDA UDI
Class IIActive
Stingray Surgical Products S02-696RU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-678TRSD45
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-680RSU30
FDA UDI
Class IIActive
Stingray Surgical Products S02-696S
FDA UDI
Class IIActive
Stingray Surgical Products S02-651RSD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-682NS
FDA UDI
Class IIActive
Stingray Surgical Products S02-680RD45
FDA UDI
Class IIActive
Stingray Surgical Products S02-653RD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-675TD45
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-695SD45
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.