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National Advanced Endoscopy Devices, Inc.

United Statesfrom the FDA registration address FDA establishment FEI 3000204191

Devices
7,296
Registrations
FDA
FDA recalls
0

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.

AI-generated from registry data, 4 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue7,296

Newest first, rows 1-50 of 7,296

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  • Aed AED2718B

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Aed AED2717B

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Aed AED2719B

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Aed 8815SB

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Aed 8810SB

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Aed 101012

    Listed Registry: GUDID Class:II
  • Aed 10121-A

    Listed Registry: GUDID Class:II
  • Aed AED26173AD

    Listed Registry: GUDID Class:II
  • Aed 101016

    Listed Registry: GUDID Class:II
  • Aed 101001

    Listed Registry: GUDID Class:II
  • Aed 101021-A

    Listed Registry: GUDID Class:II
  • Aed 101311

    Listed Registry: GUDID Class:II
  • Aed 101211

    Listed Registry: GUDID Class:II
  • Aed 101011-A

    Listed Registry: GUDID Class:II
  • Aed 101000

    Listed Registry: GUDID Class:II
  • Aed 101066

    Listed Registry: GUDID Class:II
  • Aed 101021

    Listed Registry: GUDID Class:II
  • Aed 101013T

    Listed Registry: GUDID Class:II
  • Aed 101066-L

    Listed Registry: GUDID Class:II
  • Aed 101066-S

    Listed Registry: GUDID Class:II
  • Aed 101015

    Listed Registry: GUDID Class:II
  • Aed STZ1593

    Listed Registry: GUDID Class:II
  • Aed AED11275FE

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Aed AED27071TJ

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Aed 271746

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Aed AED27071-9

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Aed 67161FZ

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Aed 67161D

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Aed A24136-47

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Aed STZ1592

    Listed Registry: GUDID Class:II
  • Aed STZ1592-45

    Listed Registry: GUDID Class:II
  • Aed STZ1594

    Listed Registry: GUDID Class:II
  • Aed STZ1593-45

    Listed Registry: GUDID Class:II
  • Aed STA1593

    Listed Registry: GUDID Class:II
  • Aed STA1592

    Listed Registry: GUDID Class:II
  • Aed STA1594

    Listed Registry: GUDID Class:II
  • Aed STZ1594-45

    Listed Registry: GUDID Class:II
  • Aed 17-1719

    Listed Registry: GUDID Class:I
  • Aed 271745

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Aed 020-017-2200H

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Aed 27174T

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Aed 271743

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Aed AED27425ZG

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Listed Registry: GUDID Class:I
  • Listed Registry: GUDID Class:I
  • Aed AED27023FG

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Aed U5740

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Aed U5780

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Aed U5790

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Aed A24131-47

    Active Regimes: 510(k) Registry: GUDID Class:II

Rows 1-50 of 7,296

Showing 1-50 of 7,296

Company details

FDA FEI number
3000204191
Address
22134 SHERMAN WAY, CANOGA PARK, CA, 91303

Frequently asked questions

How many devices does NATIONAL ADVANCED ENDOSCOPY DEVICES, INC. have in the registry?

The registry currently lists 7296 devices for NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.. Devices recorded under merged duplicate company entries are counted once.

Which registries list NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.'s devices?

Among its 50 most recently registered devices, NATIONAL ADVANCED ENDOSCOPY DEVICES, INC. has devices listed in FDA GUDID (50 devices).

What risk classes do NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.'s devices fall under?

Among its 50 most recently registered devices, the classes recorded for NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from NATIONAL ADVANCED ENDOSCOPY DEVICES, INC. in the registry?

The most recently registered devices listed for NATIONAL ADVANCED ENDOSCOPY DEVICES, INC. include AED AED2718B, AED AED2717B, AED AED2719B and AED 8815SB.

Generated automatically from registry data and not verified by a human reviewer.

This is an FDA establishment record. No EUDAMED registration is known for this company and no recalls are recorded.