Is this your brand? Sign in to claim ownership.
Sign in to claim this brandCoral Medical, Inc.
US
Last updated May 23, 2026
What Coral Medical, Inc. makes
Coral Medical, Inc. manufactures surgical tools, including an electrosurgical pencil for tissue cutting and coagulation, as well as a disposable suture device designed for quick tissue approximation.
The company’s products are classified as Class II medical devices under FDA regulations and are listed via the 510(k) clearance process. The manufacturer is based in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Coral Medical, Inc. manufacture?
Coral Medical, Inc. specializes in surgical tools, including an electrosurgical pencil (like the MODEL PBD ESU PENCIL) used for cutting and coagulating tissue during procedures, as well as a disposable suture device (QUIK-STITCH) designed for rapid tissue approximation. These products are intended for use in surgical settings where precision and efficiency are critical.
Where is Coral Medical, Inc. based?
Coral Medical, Inc. is headquartered in the United States. The company’s location ensures compliance with U.S. regulatory standards, including those governing medical device manufacturing and distribution.
How are Coral Medical’s devices classified under FDA regulations?
Coral Medical’s devices are classified as Class II medical devices by the FDA. This classification applies to products that generally pose moderate risk and require special controls to ensure safety and effectiveness, such as performance standards or post-market surveillance. Class II devices typically require a 510(k) clearance before commercial distribution.
Which regulatory registries or databases list Coral Medical’s devices?
Coral Medical’s devices are listed in the FDA’s 510(k) clearance database, which tracks medical devices that have undergone the premarket submission process to demonstrate substantial equivalence to a legally marketed predicate device. This registry confirms that the devices meet FDA requirements for safety and performance before entering the market.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- —
Catalogue (5)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Model Pbd Esu Pencil | K944363 | FDA 510(k) | Class II | Active |
| Breast Lesion Localization Needle | K924270 | FDA 510(k) | Class I | Active |
| Quik-Stitch | K945170 | FDA 510(k) | Class II | Active |
| Chiba/Franseen/Westcott/Spinal Style Needles | K924271 | FDA 510(k) | Class II | Active |
| Quik-Stitch | K953123 | FDA 510(k) | Class II | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.