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Synergetics 20.51

by Synergetics USA, Inc.

Synergetics 20.51 is a Class I device made by Synergetics USA, Inc., listed in FDA GUDID since 18 Sep 2020 (UDI-DI 10841305103983), 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 Number10841305103983 UDI-DI Date18 Sep 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  • Withdrawn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
Synergetics
Generic name
Ophthalmic soft-tissue manipulation forceps, probe-like, reusable
Model / Ref / Catalog
20.51
Primary DI / UDI-DI
10841305103983
FDA product code
MDM
GMDN term
Ophthalmic soft-tissue manipulation forceps, probe-like, reusable
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution

Related devices

Category: Ophthalmic soft-tissue manipulation forceps, probe-like, reusable

Similar devices in this category

Other devices filed under Ophthalmic soft-tissue manipulation forceps, probe-like, reusable.

Other devices from Synergetics, Inc.

See all devices from Synergetics, Inc. →

Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)