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Bausch + Lomb N5032

by Bausch & Lomb Incorporated

Bausch + Lomb N5032 is a Class I device made by Bausch & Lomb Incorporated, listed in FDA GUDID since 29 Jul 2025 (UDI-DI 00757770430277), 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 Number00757770430277 UDI-DI Date29 Jul 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  • Withdrawn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
Nasal scissors
Model / Ref / Catalog
N5032
Primary DI / UDI-DI
00757770430277
FDA product code
KBD
GMDN term
Nasal scissors
Device class
Class I
Regulation number
874.4420
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Nasal scissors

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Other devices filed under Nasal scissors.

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Properties

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