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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 89 of 96| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Stingray Surgical Products | S03-591NS | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-678TU20 | FDA UDI | Class II | Unknown |
| Stingray Surgical Products | S02-676RU45 | FDA UDI | Class II | Unknown |
| Stingray Surgical Products | G92-131 | FDA UDI | Class I | Active |
| Stingray Surgical Products | S03-697NSRS | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-677TU45 | FDA UDI | Class II | Unknown |
| Stingray Surgical Products | S02-678TU30 | FDA UDI | Class II | Unknown |
| Stingray Surgical Products | S02-676TS | FDA UDI | Class II | Unknown |
| Stingray Surgical Products | S03-539NSRU45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-674TSD45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-622 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-443RS | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-060NS | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-565NSU45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-285NSD45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-543NSRD45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-696TRSU20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-138NS | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-653TRSU45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-394NSD30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-092NS | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-678TRSD20 | FDA UDI | Class II | Unknown |
| Stingray Surgical Products | S02-680TRSU20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-636TRS | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-695RD20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-681TS | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-467SP | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-591NSD30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-330 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-394NSD20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-593NSU45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-537SPD30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-620 | FDA UDI | Class II | Unknown |
| Stingray Surgical Products | S03-545NSRD20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-265FG | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-548SPRD30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-405R | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-634TS | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-583NSD30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-695NSRSD45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-096 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-676R | FDA UDI | Class II | Unknown |
| Stingray Surgical Products | S02-634R | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-681U20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-064 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-674R | FDA UDI | Class II | Unknown |
| Stingray Surgical Products | S03-098SS | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-698D45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-675NSRSU45 | FDA UDI | Class II | Unknown |
| Stingray Surgical Products | S03-601 | FDA UDI | Class II | Active |
Related Companies
Authorised Representatives
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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. |