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Bausch + Lomb N4304

by Bausch & Lomb Incorporated

Bausch + Lomb N4304 is a Class I device made by Bausch & Lomb Incorporated, listed in FDA GUDID since 11 Apr 2025 (UDI-DI 00757770411368), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00757770411368 UDI-DI Date11 Apr 2025ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Bausch + Lomb
Generic name
Middle ear chisel
Model / Ref / Catalog
N4304
Primary DI / UDI-DI
00757770411368
FDA product code
GFI
GMDN term
Middle ear chisel
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Middle ear chisel

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Other devices filed under Middle ear chisel.

Other devices from Bausch & Lomb Incorporated

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Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)