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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 16 of 96| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Stingray Surgical Products | S03-402SPD20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-288FGU45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | G92-067 | FDA UDI | Class I | Active |
| Stingray Surgical Products | S03-545NSRU45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-698RSU45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-699TR | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-333 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-446NSR | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-469SPRD45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-695NSSD20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-648NSRS | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-655RSU30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-653RD20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-533SPRU20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-392R | FDA UDI | Class II | Unknown |
| Stingray Surgical Products | S03-581NSD45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-233FGD45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-457SPU30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-549NSU30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-680U20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-061TS | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-696TD45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-070 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-855EF | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-653D20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-699NSD45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-682SD45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-677NSD45 | FDA UDI | Class II | Unknown |
| Stingray Surgical Products | S02-384 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-286FGU20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-682TU30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-675TSU20 | FDA UDI | Class II | Unknown |
| Stingray Surgical Products | S03-537NS | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-056TS | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-590NSU45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-685NSD30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-596NSD20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-390NSRD45 | FDA UDI | Class II | Unknown |
| Stingray Surgical Products | S03-681NSD45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-374 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-674NSD30 | FDA UDI | Class II | Unknown |
| Stingray Surgical Products | S03-533SPRD45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-247FGU30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-402NSD30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-699SU45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-438NSR | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-648NSRSD20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-069 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-697R | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-235FGU20 | 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. |