Foremount Enterprise Co., Ltd.
Taichung City, TW
FOREMOUNT ENTERPRISE CO., LTD. appears in FDA device records in Taichung City, TW. FDA records list one 510(k) clearance, no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.
FDA records held for this company
510(k) clearance history
FDA records hold 1 510(k) clearance for Foremount Enterprise Co., Ltd. in 2018.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2018 | 1 |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 3010402691 | 3010402691 | FOREMOUNT ENTERPRISE CO., LTD. | No. 257, Sec. 5, Changping Rd., Taichung City 429 TW | 2026 | and 20 more, listed in full below |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
- KRIAccessory Equipment, Cardiopulmonary Bypass
- CAEAirway, Oropharyngeal, Anesthesiology
- BYEAttachment, Breathing, Positive End Expiratory Pressure
- BTCBag, Reservoir
- CATCannula, Nasal, Oxygen
- CAICircuit, Breathing (W Connector, Adaptor, Y Piece)
- BXJClip, Nose
- BYDCondenser, Heat And Moisture (Artificial Nose)
- BZAConnector, Airway (Extension)
- CAHFilter, Bacterial, Breathing-Circuit
- KBNGag, Mouth
- NVPHolding Chambers, Direct Patient Interface
- KFZHumidifier, Non-Direct Patient Interface (Home-Use)
- KZDInfusor, Pressure, For I.V. Bags
- CCWLaryngoscope, Rigid
- BSJMask, Gas, Anesthetic
- BYGMask, Oxygen
- BYFMask, Oxygen, Low Concentration, Venturi
- KGBMask, Oxygen, Non-Rebreathing
- CAPMonitor, Airway Pressure (Includes Gauge And/Or Alarm)
- BYPMouthpiece, Breathing
- CAFNebulizer (Direct Patient Interface)
- CCQNebulizer, Medicinal, Non-Ventilatory (Atomizer)
- LZAPolymer Patient Examination Glove
- BZOSet, Tubing And Support, Ventilator (W Harness)
- BTKStrap, Head, Gas Mask
- BSRStylet, Tracheal Tube
- BYXTubing, Pressure And Accessories
- CBPValve, Non-Rebreathing
- BTMVentilator, Emergency, Manual (Resuscitator)
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
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Data as of , FDA export datePage updated Source: openFDA, public domain