Steri-Tek
Fremont, CA, US
STERI-TEK appears in FDA device records in Fremont, CA. FDA records list no 510(k) clearances, no PMA records and 2 registered establishments. 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) clearances
- 0
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 2
510(k) clearance history
No 510(k) clearance records for this company in the ingested FDA data.
No 510(k) clearance records in the ingested FDA data.
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 3012448339 | 3012448339 | STERI-TEK | 48225 Lakeview Blvd, Fremont, CA 94538 US | 2026 | and 28 more, listed in full below |
| 3024987432 | 3024987432 | STERI-TEK, LLC | 1206 N Stemmons Fwy, Lewisville, TX 75067 US | 2026 |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
- QSZAbsorbable Synthetic Wound Dressing
- EOQBronchoscope (Flexible Or Rigid)
- FGYCannula, Injection
- GEJCarrier, Ligature
- LITCatheter, Angioplasty, Peripheral, Transluminal
- KRACatheter, Continuous Flush
- ENWCatheter, Nasopharyngeal
- DQYCatheter, Percutaneous
- NNKContainer, Specimen Mailer And Storage, Non-Sterile
- MGBDevice, Hemostasis, Vascular
- KRDDevice, Vascular, For Promoting Embolization
- FRODressing, Wound, Drug
- OWODrug-Eluting Sinus Stent
- GXQDura Substitute
- MQVFiller, Bone Void, Calcium Compound
- MBPFiller, Bone Void, Osteoinduction (W/O Human Growth Factor)
- FCLForceps, Biopsy, Non-Electric
- HNQHook, Ophthalmic
- DWSInstruments, Surgical, Cardiovascular
- QDKIntegrated Continuous Glucose Monitoring System For Non-Intensive Diabetes Management
- QBJIntegrated Continuous Glucose Monitoring System, Factory Calibrated
- HNNKnife, Ophthalmic
- SAHMagnetic Compression Anastomosis System
- FTMMesh, Surgical
- OWYMesh, Surgical, Collagen, Orthopaedics, Reinforcement Of Tendon
- OXEMesh, Surgical, Collagen, Staple Line Reinforcement
- MQXNeedle, Acupuncture, Single Use
- GAANeedle, Aspiration And Injection, Disposable
- HWQPasser
- NHBPolymer, Ear, Nose And Throat, Synthetic, Absorbable
- FMKSingle Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature
- LYASplint, Intranasal Septal
- GDTStaple, Removable (Skin)
- FMFSyringe, Piston
- KGXTape And Bandage, Adhesive
- PUMTemporary Catheter, Embolic Protection, Transcatheter Intracardiac Procedures
- MLYVapocoolant Device
- PTLWire, Guide, Catheter, Exempt
- KGNWound Dressing With Animal-Derived Material(S)
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