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Sign in to claim this brandSTINGRAY SURGICAL PRODUCTS
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 1701 Costa Del Sol, Boca Raton, FL, 33432
- Website
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3006059917
- DUNS Number
- —
Catalogue (4782)
Page 85 of 96| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Stingray Surgical Products | S03-543SPD30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-100NSSS | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-495NSHR | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-675TU45 | FDA UDI | Class II | Unknown |
| Stingray Surgical Products | S02-695SU45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-268FGU30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-655TRU45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-614T | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-593NS | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-263NSU20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-394SPD45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-566NS | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-683RSU20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-682TRU20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-697NSRSD45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-648SD45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-699RSU30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-390S | FDA UDI | Class II | Unknown |
| Stingray Surgical Products | S03-120NSD20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-648S | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-652RSU30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-698NS | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-069S | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-370NSS | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-652RU20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-240FGZ | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-459NSRD45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-427NSR | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-285FG | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-457SPRU20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-685RD20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-651NSSU20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-102 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-469SPRD20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-498NS | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-678TRS | FDA UDI | Class II | Unknown |
| Stingray Surgical Products | S03-450NSU30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-681TRD20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-695 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-697S | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-685RU20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-453SPRD45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-243NSD45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | G92-014 | FDA UDI | Class I | Active |
| Stingray Surgical Products | S02-648RD45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-463SPRU20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | G03-008 | FDA UDI | Class I | Active |
| Stingray Surgical Products | S03-543SPD20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-067T | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-677SD30 | FDA UDI | Class II | Unknown |
Related Companies
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Authorities
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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.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| May 23, 2012 | Z-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. |