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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 10 of 96| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Stingray Surgical Products | S03-468SPRD30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-682TRSD20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-453NSD30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-096NSS | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-675TRD20 | FDA UDI | Class II | Unknown |
| Stingray Surgical Products | S03-685TD30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-580NSD45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-697TRU30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | G42-490I | FDA UDI | Class I | Active |
| Stingray Surgical Products | S03-465NSD30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-652RSD20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-147NSU30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-086 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-438 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-459SPR | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-410R | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-459NSRU20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-678NSU30 | FDA UDI | Class II | Unknown |
| Stingray Surgical Products | S02-063T | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-467NSRD45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-458SPD30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-392SPD45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-429NS | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-681TU30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-683T | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-065TS | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-634T | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-677D45 | FDA UDI | Class II | Unknown |
| Stingray Surgical Products | S02-674TRSD45 | FDA UDI | Class II | Unknown |
| Stingray Surgical Products | S02-652TRD45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-286FGU45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-675TSU45 | FDA UDI | Class II | Unknown |
| Stingray Surgical Products | S03-681TRSU45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-404NS | FDA UDI | Class II | Active |
| Stingray Surgical Products | G42-490TCI | FDA UDI | Class I | Active |
| Stingray Surgical Products | S03-440 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-653TRSD30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-416NS | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-682TRU45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-064S | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-467NSD30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-453SPRD20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-540SP | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-394SP | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-652TR | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-070NSS | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-648NSSU30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-652TR | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-682S | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-235NSD30 | FDA UDI | Class II | Active |
Related Companies
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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. |