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Bausch + Lomb N7762

by Bausch & Lomb Incorporated United States GUDID

Product code KAA

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00757770434756 UDI-DIDate7 Aug 2025ListedStatusIn distribution

Coverage

1 jurisdiction

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  • Listed
  • Not covered

United States — GUDID listing Listed

Recalls: none on record (FDA, checked 23 Oct 2026)

Specification

GUDID · synced 23 Oct 2026

Trade Name
Bausch + Lomb
Generic Name
Vocal cord medialization implant injection needle
Model / Ref / Catalog
N7762
Primary DI / UDI-DI
00757770434756
FDA Product Code
KAA
GMDN Term
Vocal cord medialization implant injection needle
Device Class
Class I
Regulation Number
874.4420
Commercial Distribution
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

Related devices

Category: Vocal cord medialization implant injection needle

Other devices from Bausch & Lomb Incorporated

See all devices from Bausch & Lomb Incorporated →

Properties & raw data

Show properties, registry sources and raw records
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
Other properties (11)
  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No

Sources (1)

  • FDA UDI 838c528c-b3b4-4c0e-a422-9803c2d11fea 34 fields · synced 23 Oct 2026