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 69 of 96
DeviceModel / ReferenceRegistriesClassStatus
Stingray Surgical Products S02-651TD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-651D30
FDA UDI
Class IIActive
Stingray Surgical Products S03-675SU45
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-651NSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-088S
FDA UDI
Class IIActive
Stingray Surgical Products S03-651SU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-697TSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-695TRU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-697SD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-435NSR
FDA UDI
Class IIActive
Stingray Surgical Products G92-024
FDA UDI
Class IActive
Stingray Surgical Products S03-068S
FDA UDI
Class IIActive
Stingray Surgical Products S03-460SPRU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-685TRSU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-699NSRS
FDA UDI
Class IIActive
Stingray Surgical Products S02-677TSD20
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-683TD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-680NSRS
FDA UDI
Class IIActive
Stingray Surgical Products S03-698NSU30
FDA UDI
Class IIActive
Stingray Surgical Products S02-676SD45
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-102SS
FDA UDI
Class IIActive
Stingray Surgical Products S03-450SPRD30
FDA UDI
Class IIActive
Stingray Surgical Products S03-409R
FDA UDI
Class IIActive
Stingray Surgical Products S02-648TU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-697NSRSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-396SPRD30
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-485NSHR
FDA UDI
Class IIActive
Stingray Surgical Products S03-237NSD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-427
FDA UDI
Class IIActive
Stingray Surgical Products S03-118NSU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-597NSU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-652TRSU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-678SU30
FDA UDI
Class IIUnknown
Stingray Surgical Products S02-683D20
FDA UDI
Class IIActive
Stingray Surgical Products S03-465SPRU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-680SD45
FDA UDI
Class IIActive
Stingray Surgical Products S03-629
FDA UDI
Class IIActive
Stingray Surgical Products S03-538SPRU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-457SPRD30
FDA UDI
Class IIActive
Stingray Surgical Products S02-070S
FDA UDI
Class IIActive
Stingray Surgical Products S03-648U30
FDA UDI
Class IIActive
Stingray Surgical Products S03-653NSRSU20
FDA UDI
Class IIActive
Stingray Surgical Products S03-681TRU30
FDA UDI
Class IIActive
Stingray Surgical Products S03-584NSU45
FDA UDI
Class IIActive
Stingray Surgical Products S03-680NSRSU20
FDA UDI
Class IIActive
Stingray Surgical Products S02-402R
FDA UDI
Class IIUnknown
Stingray Surgical Products S03-626
FDA UDI
Class IIActive
Stingray Surgical Products S03-539NSRD20
FDA UDI
Class IIActive
Stingray Surgical Products S03-457NS
FDA UDI
Class IIActive
Stingray Surgical Products S03-538NS
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.