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Sign in to claim this brandNATIONAL ADVANCED ENDOSCOPY DEVICES, INC.
US
Last updated September 17, 2026
What NATIONAL ADVANCED ENDOSCOPY DEVICES, INC. makes
National Advanced Endoscopy Devices, Inc. manufactures reusable endoscopic instruments, including rigid and flexible tissue manipulation forceps, reusable arthroscopic and ENT surgical procedure kits, endoscopic electrosurgical electrodes, endoscope sheaths, and suturing needle holders. Their product line also covers reusable rigid optical arthroscopes, designed for surgical procedures requiring precise visualisation and manipulation.
The company’s devices are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database. The portfolio is regulated under US medical device laws, with individual products authorised through the relevant FDA clearance pathways.
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 National Advanced Endoscopy Devices, Inc. manufacture?
National Advanced Endoscopy Devices, Inc. specialises in reusable endoscopic instruments. Their product line includes rigid and flexible endoscopic tissue manipulation forceps, reusable arthroscopic and ENT surgical procedure kits, endoscopic electrosurgical electrodes, endoscope sheaths, and suturing needle holders. They also produce reusable rigid optical arthroscopes, which are used in surgeries requiring detailed visualisation and precise manipulation.
Where is National Advanced Endoscopy Devices, Inc. based?
The company is based in the United States. This location aligns with its regulatory compliance under US medical device laws, ensuring its products meet the necessary standards for distribution and use within the country.
Which regulatory registries list devices manufactured by National Advanced Endoscopy Devices, Inc.?
Devices from National Advanced Endoscopy Devices, Inc. are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify their products under US medical device regulations, ensuring transparency and traceability for healthcare providers.
How are the devices produced by National Advanced Endoscopy Devices, Inc. classified under FDA regulations?
The company’s devices fall under FDA’s Class I and Class II categories. Class I generally includes low-risk devices requiring general controls, while Class II involves special controls to ensure safety and effectiveness. The classification determines the regulatory pathway each product must follow for authorisation.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- 22134 SHERMAN WAY, CANOGA PARK, CA, 91303
- Website
- —
- —
- —
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- Phone
- —
- PRRC Contact
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- EUDAMED SRN
- —
- FDA FEI Number
- 3000204191
- DUNS Number
- —
Catalogue (7162)
Page 98 of 144| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Speedlock | 8511-07-R/1358 | FDA UDI | Class II | Active |
| Speedlock | 8516-12-45/8510-00 | FDA UDI | Class II | Active |
| Speedlock | 8514-18-45 | FDA UDI | Class II | Active |
| Speedlock | 8514-21-30/1366 | FDA UDI | Class II | Active |
| Speedlock | 8514-05-26-R/8511-01 | FDA UDI | Class II | Active |
| Speedlock | 8510-46-26-R/1358 | FDA UDI | Class II | Active |
| Aed | 120-497-350 | FDA UDI | Class I | Active |
| Instrument Ligature Passing and Knot Tying | KP1618 | FDA UDI | Class I | Active |
| Speedlock | 8511-03/1366 | FDA UDI | Class II | Active |
| Aed | 5710FXXL | FDA UDI | Class II | Active |
| Speedlock | 8515-09-26-R/8511-00 | FDA UDI | Class II | Active |
| Speedlock | 8514-85/8510-00 | FDA UDI | Class II | Active |
| Speedlock | 8514-01-26-R/D1368 | FDA UDI | Class II | Active |
| Speedlock | 8512-33-R/1362 | FDA UDI | Class II | Active |
| Speedlock | 8512-16-30-R/8510-01 | FDA UDI | Class II | Active |
| Speedlock | 8512-25-30-R/D1368 | FDA UDI | Class II | Active |
| Speedlock | 8512-25-45/8511-02 | FDA UDI | Class II | Active |
| Aed | 17-1824 DK | FDA UDI | Class I | Active |
| Speedlock | 8514-61-26-R/1362 | FDA UDI | Class II | Active |
| Aed | 17-1770 | FDA UDI | Class I | Active |
| Mini Precise | xp1413 | FDA UDI | Class II | Active |
| Mini Precise | xpw1353 | FDA UDI | Class II | Active |
| Speedlock | 8514-69-30-R/8511-00 | FDA UDI | Class II | Active |
| Speedlock | 8510-13-26/1358 | FDA UDI | Class II | Active |
| Speedlock | 8514-93-R/8511-01 | FDA UDI | Class II | Active |
| Speedlock | 8512-17-26/8511-02 | FDA UDI | Class II | Active |
| Speedlock | 8510-37-30-R/8511-01 | FDA UDI | Class II | Active |
| Aed | 32-4155 | FDA UDI | Class II | Active |
| Speedlock | 8517-06-26-R/1358 | FDA UDI | Class II | Active |
| Speedlock | 8511-09-45-I | FDA UDI | Class II | Active |
| Speedlock | 8512-41-30-R/1362 | FDA UDI | Class II | Active |
| Aed | 32-4303 | FDA UDI | Class II | Active |
| Speedlock | 8514-11/1366 | FDA UDI | Class II | Active |
| Speedlock | 8514-05/1358 | FDA UDI | Class II | Active |
| Speedlock | 8512-65-45/8510-00 | FDA UDI | Class II | Active |
| Speedlock | 8510-33-R/1362 | FDA UDI | Class II | Active |
| Aed | 120-403-350 | FDA UDI | Class I | Active |
| Speedlock | 8511-37-30-R/8510-02 | FDA UDI | Class II | Active |
| Speedlock | 8510-41-26-R/8511-01 | FDA UDI | Class II | Active |
| Speedlock | 8512-05-45-R | FDA UDI | Class II | Active |
| Aed | 501.03 | FDA UDI | Class I | Active |
| Speedlock | 8514-49-26/1366 | FDA UDI | Class II | Active |
| Aed | 270 | FDA UDI | Class I | Active |
| Speedlock | 8510-47 | FDA UDI | Class II | Active |
| Aed | 32-4408 | FDA UDI | Class II | Active |
| Speedlock | 8515-13-45 | FDA UDI | Class II | Active |
| Aed | AED116800 | FDA UDI | Class II | Active |
| Speedlock | 8511-05-30-R/1358 | FDA UDI | Class II | Active |
| Speedlock | 8513-27-I | FDA UDI | Class II | Active |
| Speedlock | 8511-07-45 | FDA UDI | Class II | Active |
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