Utrata Kershner Capsulorhexis Cystotome Forceps T14-5385

by Sontec Instruments, Inc.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00192896074026 UDI-DI	Date19 Sep 2018Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Utrata Kershner Capsulorhexis Cystotome Forceps
Generic Name: Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable
Model / Ref / Catalog: T14-5385

Primary DI / UDI-DI: 00192896074026
FDA Product Code: HNR
GMDN Term: Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable

Device Class: Class I
Regulation Number: 886.4350
GUDID distribution status: In Commercial Distribution

Other devices from Sontec Instruments, Inc.

Adson Tissue Forceps 140-302DLQ

Class I
Micro Skinner Forceps 140-519M

Class I
Gum Scissors 475-153Q

Class I
Thumb Dressing Forceps 136-610Q

Class I
Thumb Dressing Forceps 136-615Q

Class I
Thumb Dressing Forceps 136-619Q

Class I

See all devices from Sontec Instruments, Inc. →

Properties

Prescription Use
Premarket Exempt
Lot / Batch Number

Other properties (11)

Sterile: No
Single Use: No
Implantable: No
Contains Latex: No
Over-the-Counter: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Serial Number: No
Expiration Date: No
Manufacturing Date: No