FDA Device Intelligence
Home › SHANGHAI MEDIWORKS PRECISION INSTRUMENTS CO.,LTD. › MediWorks

MediWorks

SHANGHAI MEDIWORKS PRECISION INSTRUMENTS CO.,LTD. · Model T170(R) · UDI-DI 06945087517017

HKY
1
510(k) clearances
11
Adverse events
2
Recalls
63
Facilities

Description

Tonometer is indicated for Intraocular Pressure (IOP) measurement .

Recalls

DateFirmReason
2014-09-08Instrumed International, Inc.The reason these devices are being withdrawn from the market by Instrumed is that Instrumed did not market these devices prior to September 26, 1976, and therefore, does not meet a
2014-09-08Instrumed International, Inc.The reason these devices are being withdrawn from the market by Instrumed is that Instrumed did not market these devices prior to September 26, 1976, and therefore, does not meet a

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.