Data / Medical devices / United States / Alira Medical Devices LLC
Alira Medical Devices LLC: FDA-registered device maker in Rancho Cucamonga, CA, United States, 2 510(k) clearances
Alira Medical Devices LLC is registered with the FDA (registration 3022320321) in Rancho Cucamonga, CA, United States. It lists 98 device types. The FDA files 2 510(k) clearances under its listings, the newest dated December 1, 2009. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3022320321
- Address
- 8560 Vineyard Ave Ste 507, Rancho Cucamonga, CA, United States, 91730
- Owner or operator
- ALIRA MEDICAL DEVICES LLC (10084932)
- Roles
- Manufacturer for export, Repackager or relabeler, Specification developer
- First device listed
- April 16, 2022
- Registered through
- 2026
- Brand names listed
- ACCESSORIES, CATHETER, ADAPTOR, CATHETER, ALIRA MEDICAL DEVICES, ALIRA'S JOINT, KNEE, EXTERNAL LIMB COMPONENT, APPLIER, HEMOSTATIC CLIP, Adipose; Boost Adipose Micronizer; Filter Turbo Micronizer; Manual Injector, Aira 's LOUPE, DIAGNOSTIC/SURGICAL, Alira and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|
| Accessories, Catheter | KGZ | 1 | Specification developer | accessdata.fda.gov |
| Adaptor, Catheter | GCE | 1 | Repackager or relabeler | accessdata.fda.gov |
| Adaptor, Holder, Syringe | IQG | 1 | Repackager or relabeler | accessdata.fda.gov |
| Applier, Hemostatic Clip | HBT | 1 | Specification developer | accessdata.fda.gov |
| Applier, Surgical, Clip | GDO | 1 | Specification developer | accessdata.fda.gov |
| Bag, Intestine | KGY | 1 | Repackager or relabeler | accessdata.fda.gov |
| Block, Cutting, Ent, Non-Sterile | NNR | 1 | Repackager or relabeler | accessdata.fda.gov |
| Bottle, Collection, Vacuum | KDQ | 2 | Repackager or relabeler | accessdata.fda.gov |
| Bur, Surgical, General & Plastic Surgery | GFF | 1 | Repackager or relabeler | accessdata.fda.gov |
| Burr, Corneal, Manual | HOF | 1 | Specification developer | accessdata.fda.gov |
| Cable, Electrode | IKD | 2 | Repackager or relabeler | accessdata.fda.gov |
| Caliper | KTZ | 1 | Specification developer | accessdata.fda.gov |
| Camera, Cine, Endoscopic, Without Audio | FWL | 1 | Repackager or relabeler | accessdata.fda.gov |
| Camera, Cine, Microsurgical, Without Audio | FWJ | 1 | Specification developer | accessdata.fda.gov |
| Cannula, Injection | FGY | 1 | Repackager or relabeler | accessdata.fda.gov |
| Cannula, Surgical, General & Plastic Surgery | GEA | 1 | Specification developer | accessdata.fda.gov |
| Cap, Surgical | FYF | 1 | Repackager or relabeler | accessdata.fda.gov |
| Cart, Emergency, Cardiopulmonary (Excluding Equipment) | BZN | 1 | Repackager or relabeler | accessdata.fda.gov |
| Centrifuge For Preparation Of Cell Concentrate And/Or Plasma Concentrate | QBV | 1 | Specification developer | accessdata.fda.gov |
| Chisel (Osteotome) | KDG | 1 | Specification developer | accessdata.fda.gov |
| Clamp, Surgical, General & Plastic Surgery | GDJ | 1 | Specification developer | accessdata.fda.gov |
| Compressor, Air, Portable | BTI | 2 | Repackager or relabeler | accessdata.fda.gov |
| Contractor, Surgical | FZR | 1 | Repackager or relabeler | accessdata.fda.gov |
| Crimper, Pin | HXQ | 1 | Specification developer | accessdata.fda.gov |
| Curette | HTF | 1 | Specification developer | accessdata.fda.gov |
| Curette, Surgical, General Use | FZS | 1 | Repackager or relabeler | accessdata.fda.gov |
| Cutter, Surgical | FZT | 1 | Repackager or relabeler | accessdata.fda.gov |
| Dermatome | GFD | 1 | Repackager or relabeler | accessdata.fda.gov |
| Dilator, Catheter | GCC | 1 | Repackager or relabeler | accessdata.fda.gov |
| Dissector, Surgical, General & Plastic Surgery | GDI | 1 | Repackager or relabeler | accessdata.fda.gov |
| Drape, Surgical, Exempt | PUI | 2 | Repackager or relabeler | accessdata.fda.gov |
| Dress, Surgical | FYE | 1 | Repackager or relabeler | accessdata.fda.gov |
| Electrode, Electrocardiograph, Multi-Function | MLN | 2 | Repackager or relabeler | accessdata.fda.gov |
| Electrosurgical, Cutting & Coagulation & Accessories | GEI | 2 | Repackager or relabeler | accessdata.fda.gov |
| Elevator | HTE | 1 | Specification developer | accessdata.fda.gov |
| Elevator, Surgical, General & Plastic Surgery | GEG | 1 | Repackager or relabeler | accessdata.fda.gov |
| Epilator, High Frequency, Needle-Type | KCW | 1 | Repackager or relabeler | accessdata.fda.gov |
| Expander, Surgical, Skin Graft | FZW | 1 | Repackager or relabeler | accessdata.fda.gov |
| Filters, Cell Collection, Tissue Processing | KET | 1 | Repackager or relabeler | accessdata.fda.gov |
| Forceps, General & Plastic Surgery | GEN | 1 | Specification developer | accessdata.fda.gov |
| Gouge, Surgical, General & Plastic Surgery | GDH | 1 | Specification developer | accessdata.fda.gov |
| Handle, Scalpel | GDZ | 1 | Specification developer | accessdata.fda.gov |
| Head, Surgical, Hammer | GFB | 1 | Repackager or relabeler | accessdata.fda.gov |
| Holder, Needle, Gastroenterologic | FHQ | 1 | Specification developer | accessdata.fda.gov |
| Hook, Bone | KIK | 1 | Repackager or relabeler | accessdata.fda.gov |
| Hook, Surgical, General & Plastic Surgery | GDG | 1 | Specification developer | accessdata.fda.gov |
| Instrument, Manual, Surgical, General Use | MDM | 1 | Repackager or relabeler | accessdata.fda.gov |
| Instrument, Surgical, Disposable | KDC | 1 | Repackager or relabeler | accessdata.fda.gov |
| Joint, Knee, External Limb Component | ISY | 1 | Repackager or relabeler | accessdata.fda.gov |
| Kit, Surgical Instrument, Disposable | KDD | 1 | Repackager or relabeler | accessdata.fda.gov |
| Knife, Amputation | GDN | 1 | Repackager or relabeler | accessdata.fda.gov |
| Knife, Ent | KTG | 1 | Specification developer | accessdata.fda.gov |
| Knife, Surgical | EMF | 1 | Repackager or relabeler | accessdata.fda.gov |
| Laryngoscope, Rigid | CCW | 1 | Manufacturer for export | accessdata.fda.gov |
| Lavage, Jet | FQH | 2 | Repackager or relabeler | accessdata.fda.gov |
| Light, Fiber Optic, Dental | EAY | 1 | Specification developer | accessdata.fda.gov |
| Light, Surgical, Accessories | FTA | 2 | Repackager or relabeler | accessdata.fda.gov |
| Light, Surgical, Carrier | FSZ | 2 | Repackager or relabeler | accessdata.fda.gov |
| Light, Surgical, Connector | FSX | 2 | Repackager or relabeler | accessdata.fda.gov |
| Light, Surgical, Endoscopic | FSW | 2 | Repackager or relabeler | accessdata.fda.gov |
| Light, Surgical, Instrument | FSQ | 2 | Specification developer | accessdata.fda.gov |
| Loupe, Diagnostic/Surgical | FSP | 1 | Repackager or relabeler | accessdata.fda.gov |
| Mallet, Surgical, General & Plastic Surgery | GFJ | 1 | Repackager or relabeler | accessdata.fda.gov |
| Marker, Skin | FZZ | 1 | Repackager or relabeler | accessdata.fda.gov |
| Material, External Aesthetic Restoration, No Adhesive | NOK | 1 | Repackager or relabeler | accessdata.fda.gov |
| Motor, Surgical Instrument, Ac-Powered | GEY | 1 | Repackager or relabeler | accessdata.fda.gov |
| Motor, Surgical Instrument, Pneumatic Powered | GET | 1 | Repackager or relabeler | accessdata.fda.gov |
| Needle, Aspiration And Injection, Disposable | GAA | 1 | Repackager or relabeler | accessdata.fda.gov |
| Needle, Suturing, Disposable | GAB | 1 | Repackager or relabeler | accessdata.fda.gov |
| Needle, Suturing, Reusable | GDL | 1 | Repackager or relabeler | accessdata.fda.gov |
| Orthopedic Manual Surgical Instrument | LXH | 1 | Repackager or relabeler | accessdata.fda.gov |
| Osteotome, Manual | GFI | 1 | Repackager or relabeler | accessdata.fda.gov |
| Passer, Wire, Orthopedic | HXI | 1 | Repackager or relabeler | accessdata.fda.gov |
| Probe | HXB | 1 | Specification developer | accessdata.fda.gov |
| Punch, Surgical | LRY | 1 | Specification developer | accessdata.fda.gov |
| Rasp | HTR | 1 | Specification developer | accessdata.fda.gov |
| Rasp, Surgical, General & Plastic Surgery | GAC | 1 | Repackager or relabeler | accessdata.fda.gov |
| Retainer, Surgical | GCZ | 1 | Specification developer | accessdata.fda.gov |
| Retractor | GAD | 1 | Specification developer | accessdata.fda.gov |
| Saw, Nasal | KBC | 1 | Repackager or relabeler | accessdata.fda.gov |
| Saw, Powered, And Accessories | HAB | 1 | Specification developer | accessdata.fda.gov |
| Scissors, General, Surgical | LRW | 1 | Specification developer | accessdata.fda.gov |
| Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear) | HOY | 1 | Specification developer | accessdata.fda.gov |
| Shoes, Operating-Room | FXW | 1 | Repackager or relabeler | accessdata.fda.gov |
| Solvent, Adhesive Tape | KOX | 1 | Repackager or relabeler | accessdata.fda.gov |
| Spatula, Orthopedic | HXR | 1 | Repackager or relabeler | accessdata.fda.gov |
| Spatula, Surgical, General & Plastic Surgery | GAF | 1 | Repackager or relabeler | accessdata.fda.gov |
| Speculum, Ent | EPY | 1 | Specification developer | accessdata.fda.gov |
| Stapler, Skin | QQS | 1 | Repackager or relabeler | accessdata.fda.gov |
| Starter, Bone Screw | HWD | 1 | Repackager or relabeler | accessdata.fda.gov |
| Suction Control, Intracardiac, Cardiopulmonary Bypass | DWD | 2 | Repackager or relabeler | accessdata.fda.gov |
| Suture, Nonabsorbable, Steel, Monofilament And Multifilament, Sterile, Exempt | PTX | 2 | Repackager or relabeler | accessdata.fda.gov |
| System, Suction, Lipoplasty For Removal | QPB | 2 | Repackager or relabeler | accessdata.fda.gov |
| Tape, Measuring, Rulers And Calipers | FTY | 1 | Specification developer | accessdata.fda.gov |
| Tray, Surgical | LRP | 1 | Specification developer | accessdata.fda.gov |
| Tray, Surgical, Instrument | FSM | 1 | Specification developer | accessdata.fda.gov |
| Tray, Surgical, Needle | FSH | 1 | Repackager or relabeler | accessdata.fda.gov |
| Tube, Aspirating, Flexible, Connecting | BYY | 2 | Repackager or relabeler | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|
| December 1, 2009 | K092634 | OBS DISPOSABLE ELECTROSURGICAL PENCILS, MODELS: OBS-DB, OBS-DR, OBS-DF | GEI | Substantially Equivalent | Jiangmen City Xinhui Baisheng Medical Equipment CO | accessdata.fda.gov |
| November 19, 2001 | K012236 | STARS2000 POWER CANNULA | QPB | Substantially Equivalent | Kmi Kolster Methods, Inc. | accessdata.fda.gov |
Compare with other makers
Updated December 1, 2009. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.