Ophta Sil (R), Punctal Plugs and Inserters

FDA 510(k) K911108 · G.W.B. Intl., Ltd.

Substantially Equivalent

510(k) numberK911108

Submission

Device name
Ophta Sil (R), Punctal Plugs and Inserters
Applicant
G.W.B. Intl., Ltd.
Sudbury, MA, US
Received
March 4, 1991
Decision date
May 13, 1991
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
LZU – Plug, Punctum
Device class
Unclassified

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K241229Hello,eyes® BIO PlugLZU · Traditional Bio Optics Co., Ltd.06/28/2024SE
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K213988SOFT PLUG Extended Duration 180 Tapered Canalicular PlugLZU · Traditional Oasis Medical, Inc.06/03/2022SE
K190210Tear Pool Dissolvable Punctum PlugsLZU · Traditional Alphamed, Inc.10/24/2019SE
K162361Soft Plug Extended Duration 180 Canalicular PlugLZU · Traditional Oasis Medical, Inc.04/17/2017SE
K161673LacriPro Punctum PlugLZU · Traditional Lacrimedics, Inc.11/18/2016SE
K150288PDO Absorbable Punctum PlugLZU · Traditional Riverpoint Medical08/28/2015SE
K140352VeraplugLZU · Traditional Krishna Imports Inc Dba Stephens Instruments11/13/2014SE
K140711Comfortear Lacrisolve Absorbable Punctum Plug, Lacrisolve Absorbable Punctum Plug…LZU · Traditional Paragon Bioteck, Inc.06/20/2014SE
K140026Collasyn Plug for the Lacrimal Efficiency TestLZU · Traditional Lacrimedics, Inc.06/03/2014SE

More from Lacrimedics, Inc.

510(k)DeviceDecision
K955671Ritleng Bican.Lacr.Sets/Self Thread. Monokas(Chg.In Ster.)OKS · Traditional 03/06/1996SE
K954094Ophta Sil- Punctal Plugs (Modification)LZU · Traditional 10/05/1995SE
K950569Ophta Sil {Self-Threading Monoka (Ritleng Type)}LZU · Traditional 03/14/1995SE
K940508Ophta Sil (Ritleng Probe and Lacrimal Intubation Set)OKS · Traditional 05/04/1994SE
K911110Ophta Sil(R), Enulceation/Evisceration ImplantsHPZ · Traditional 06/18/1991SE
K911109Ophta Sil (R), Lachrymal Intubation SetsOKS · Traditional 05/01/1991SE
K896029Digital Ultrasound Imaging System Dub 20IYO · Traditional 01/12/1990SE

Questions and answers

When was Ophta Sil (R), Punctal Plugs and Inserters cleared by the FDA?

Ophta Sil (R), Punctal Plugs and Inserters (K911108) received a 510(k) decision of Substantially Equivalent on May 13, 1991, 70 days after the submission was received.

What is the product code of K911108?

The FDA product code is LZU – Plug, Punctum, a Unclassified device.