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ENT Pocket Light PL4 Blue

by C F M Technologies Inc

ENT Pocket Light PL4 Blue (PL4-BL) is an endaural surgical curette (FDA Class I) made by C F M Technologies Inc, listed in FDA GUDID since 3 Jan 2020 (UDI-DI 00850013958054), 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 Number00850013958054 UDI-DI Date3 Jan 2020ListedStatusListed 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  • Withdrawn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
ENT Pocket Light
Generic name
Endaural surgical curette, single-use
Model / Ref / Catalog
PL4 BLUE, PL4-BL
Primary DI / UDI-DI
00850013958054
FDA product code
JYG, ERA
GMDN term
Endaural surgical curette, single-use
Device class
Class I
Regulation number
874.4420, 874.4770
GUDID distribution status
In Commercial Distribution

Related devices

Category: Ear speculum, reusableEndaural surgical curette, reusableOtoscope, directEndaural surgical curette, single-use

Similar devices

Other devices filed under FDA product code JYG (Curette, Ear).

Other devices from C F M Technologies Inc

See all devices from C F M Technologies Inc →

Properties

  • Over-the-counter
  • Convenience kit
  • Premarket exempt
Other properties (12, all answered No)