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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 18 of 96| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Stingray Surgical Products | S03-453NSRD20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-678NSSD45 | FDA UDI | Class II | Unknown |
| Stingray Surgical Products | S03-235FGD20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-463SPRD20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-653SU30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-678SU30 | FDA UDI | Class II | Unknown |
| Stingray Surgical Products | S03-540NSR | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-697NSSD30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-698RS | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-699SU20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-648NSRSU30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-676TRSU20 | FDA UDI | Class II | Unknown |
| Stingray Surgical Products | S02-680U30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-685RSU45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-651SU30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-677RS | FDA UDI | Class II | Unknown |
| Stingray Surgical Products | S03-677U45 | FDA UDI | Class II | Unknown |
| Stingray Surgical Products | S03-677NSRSU45 | FDA UDI | Class II | Unknown |
| Stingray Surgical Products | S03-578NSU20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-675SD20 | FDA UDI | Class II | Unknown |
| Stingray Surgical Products | S03-653S | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-696TSD30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-652NS | FDA UDI | Class II | Active |
| Stingray Surgical Products | G92-063 | FDA UDI | Class I | Active |
| Stingray Surgical Products | S02-683TSU45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-469NSRD45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-681D30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-677 | FDA UDI | Class II | Unknown |
| Stingray Surgical Products | S03-597NS | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-695TRD20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-678SD20 | FDA UDI | Class II | Unknown |
| Stingray Surgical Products | S03-537NSD45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-538SPRU45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-362S | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-240FGU20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-533NS | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-676TRSD20 | FDA UDI | Class II | Unknown |
| Stingray Surgical Products | S03-061 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-682RSD45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-675T | FDA UDI | Class II | Unknown |
| Stingray Surgical Products | S03-674TRU20 | FDA UDI | Class II | Unknown |
| Stingray Surgical Products | S03-548NSRD45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-082NSSS | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-088SS | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-061S | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-648 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-537SPRU45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-538SPD45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-549NSD45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-240FG | FDA UDI | Class II | Active |
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. |