PRO-TECH Design & Mfg, Inc.
Santa Fe Springs, CA, US
PRO-TECH Design & Mfg, Inc. appears in FDA device records in Santa Fe Springs, CA. FDA records list no 510(k) clearances, no PMA records and 3 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
- 3
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 |
|---|---|---|---|---|---|
| 2032521 | 3003574398 | PRO-TECH DESIGN & MFG., INC. | 14561 MARQUARDT AVE., SANTA FE SPRINGS, CA 90670 US | 2026 | and 52 more, listed in full below |
| 3010531069 | 3010531069 | PRO-TECH Design & Mfg, Inc. | 4041 Express Street, Arlington, TX 76001 US | 2026 | and 19 more, listed in full below |
| 3013023969 | 3013023969 | PRO-TECH Design & Mfg, Inc. | 13719 Borate St, Santa Fe Springs, CA 90670 US | 2026 | and 2 more, listed in full below |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
- IQGAdaptor, Holder, Syringe
- BTQAirway, Nasopharyngeal
- KTTAppliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
- KWPAppliance, Fixation, Spinal Interlaminal
- HRXArthroscope
- DWFCatheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
- JQCCentrifuges (Micro, Ultra, Refrigerated) For Clinical Use
- GXRCover, Burr Hole
- NIKDefibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)
- DREDilator, Vessel, For Percutaneous Catheterization
- NVNDrug Eluting Permanent Right Ventricular (Rv) Or Right Atrial (Ra) Pacemaker Electrodes
- GCQEndoscope, Flexible
- MBIFastener, Fixation, Nondegradable, Soft Tissue
- OAGGarment, Storage, Peritoneal Dialysis Catheter
- NWWHysteroscope Accessories
- LWSImplantable Cardioverter Defibrillator (Non-Crt)
- DXYImplantable Pacemaker Pulse-Generator
- LWPImplantable Pulse Generator, Pacemaker (Non-Crt)
- DWSInstruments, Surgical, Cardiovascular
- MAXIntervertebral Fusion Device With Bone Graft, Lumbar
- KDDKit, Surgical Instrument, Disposable
- HNNKnife, Ophthalmic
- GCJLaparoscope, General & Plastic Surgery
- HETLaparoscope, Gynecologic (And Accessories)
- FQHLavage, Jet
- LZCMedical Glove, Specialty
- LXCMonitor, Pressure, Intracompartmental
- BSPNeedle, Conduction, Anesthetic (W/Wo Introducer)
- MNIOrthosis, Spinal Pedicle Fixation
- MNHOrthosis, Spondylolisthesis Spinal Fixation
- NVYPermanent Defibrillator Electrodes
- DTBPermanent Pacemaker Electrode
- GXIProbe, Radiofrequency Lesion
- KRGProgrammer, Pacemaker
- FWMProsthesis, Breast, Inflatable, Internal, Saline
- FTRProsthesis, Breast, Noninflatable, Internal, Silicone Gel-Filled
- KWYProsthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented
- LZOProsthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
- LPHProsthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
- JWHProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
- HSDProsthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented
- KWSProsthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented
- KWDProsthesis, Toe, Hemi-, Phalangeal
- JWJProsthesis, Wrist, 3 Part Metal-Plastic-Metal Articulation, Semi-Constrained
- KXEProsthesis, Wrist, Hemi-, Ulnar
- NKEPulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)
- NVZPulse Generator, Permanent, Implantable
- HWCScrew, Fixation, Bone
- FPASet, Administration, Intravascular
- NHLStimulator, Electrical, Implanted, For Parkinsonian Symptoms
- MHYStimulator, Electrical, Implanted, For Parkinsonian Tremor
- GZFStimulator, Peripheral Nerve, Implanted (Pain Relief)
- GZBStimulator, Spinal-Cord, Implanted (Pain Relief)
- LGWStimulator, Spinal-Cord, Totally Implanted For Pain Relief
- DRBStylet, Catheter
- FMFSyringe, Piston
- MUUSystem, Suction, Lipoplasty
- NKBThoracolumbosacral Pedicle Screw System
- JKATubes, Vials, Systems, Serum Separators, Blood Collection
- HTNWasher, Bolt Nut
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.
Where there is a record, this is where it appears: what was checked, when it was checked, and the current status. An MDM Verified badge on another website links to a verify address on this domain that resolves to this section. A badge that does not resolve here is not ours.
MDM coverage
MDM coverage of this company lists here, newest first. Submit news.
Is this your company?
This page is built from public FDA records. Company pages are free and factual, and stay free whether or not anyone claims them. Membership never changes editorial coverage or vetting outcomes.
Claiming lets PRO-TECH Design & Mfg, Inc. edit what it says about itself and list the categories it works in. It grants no badge: claiming is not verification.
Data as of , FDA export datePage updated Source: openFDA, public domain