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Synergetics 55.23.23

by Synergetics USA, Inc.

Synergetics 55.23.23 is a Class II device made by Synergetics USA, Inc., listed in FDA GUDID since 15 Aug 2016 (UDI-DI 20841305106646), 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 Number20841305106646 UDI-DI Date15 Aug 2016ListedStatusListed 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  • Withdrawn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
Synergetics
Generic name
Ophthalmic laser system beam guide
Model / Ref / Catalog
55.23.23
Primary DI / UDI-DI
20841305106646
FDA product code
HQB
GMDN term
Ophthalmic laser system beam guide
Device class
Class II
Regulation number
886.4690
GUDID distribution status
In Commercial Distribution

Related devices

Category: Ophthalmic laser system beam guide

Similar devices in this category

Other devices filed under Ophthalmic laser system beam guide.

Other devices from Synergetics, Inc.

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Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)