Data / Medical devices / United States / Stallion Medical, Inc.
Stallion Medical, Inc.: FDA-registered device maker in San Diego, CA, United States, 8 510(k) clearances
Stallion Medical, Inc. is registered with the FDA (registration 2031962) in San Diego, CA, United States. It lists 70 device types. The FDA files 8 510(k) clearances under its listings, the newest dated May 3, 2013. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 2031962
- FEI number
- 3002445546
- Address
- 3085 Beyer Blvd Suite A-105, San Diego, CA, United States, 92154
- Owner or operator
- STALLION MEDICAL, INC. (9012225)
- Roles
- Repackager or relabeler
- First device listed
- March 24, 2000
- Registered through
- 2026
- Brand names listed
- Analyzer, CALIPER, CANNULA OPHTHALMIC, CLAMP, CORNEAL MARKER, CURETTE, Chart, Visual Acuity, Corneo scleral punch and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|
| Accessory, Surgical Apparel | LYU | 1 | Repackager or relabeler | accessdata.fda.gov |
| Caliper, Ophthalmic | HOE | 1 | Repackager or relabeler | accessdata.fda.gov |
| Cannula, Ophthalmic | HMX | 1 | Repackager or relabeler | accessdata.fda.gov |
| Chair, Ophthalmic, Ac-Powered | HME | 1 | Repackager or relabeler | accessdata.fda.gov |
| Chair, Ophthalmic, Manual | HMD | 1 | Repackager or relabeler | accessdata.fda.gov |
| Chart, Visual Acuity | HOX | 1 | Repackager or relabeler | accessdata.fda.gov |
| Chisel, Surgical, Manual | FZO | 1 | Repackager or relabeler | accessdata.fda.gov |
| Clamp, Eyelid, Ophthalmic | HOD | 1 | Repackager or relabeler | accessdata.fda.gov |
| Clamp, Muscle, Ophthalmic | HOB | 1 | Repackager or relabeler | accessdata.fda.gov |
| Conformer, Ophthalmic | HQN | 2 | Repackager or relabeler | accessdata.fda.gov |
| Curette, Ophthalmic | HNZ | 1 | Repackager or relabeler | accessdata.fda.gov |
| Depressor, Orbital | HNX | 1 | Repackager or relabeler | accessdata.fda.gov |
| Device, Measuring, Lens Radius, Ophthalmic | HLF | 1 | Repackager or relabeler | accessdata.fda.gov |
| Dilator, Lachrymal | HNW | 1 | Repackager or relabeler | accessdata.fda.gov |
| Exophthalmometer | HLS | 1 | Repackager or relabeler | accessdata.fda.gov |
| Forceps, Ophthalmic | HNR | 1 | Repackager or relabeler | accessdata.fda.gov |
| Frame, Spectacle | HQZ | 1 | Repackager or relabeler | accessdata.fda.gov |
| Frame, Trial, Ophthalmic | HPA | 1 | Repackager or relabeler | accessdata.fda.gov |
| Holder, Needle, Gastroenterologic | FHQ | 1 | Repackager or relabeler | accessdata.fda.gov |
| Hook, Ophthalmic | HNQ | 1 | Repackager or relabeler | accessdata.fda.gov |
| Implant, Eye Sphere | HPZ | 2 | Repackager or relabeler | accessdata.fda.gov |
| Implant, Orbital, Extra-Ocular | HQX | 2 | Repackager or relabeler | accessdata.fda.gov |
| Instrument, Measuring, Lens, Ac-Powered | HLM | 1 | Repackager or relabeler | accessdata.fda.gov |
| Keratoscope, Ac-Powered | HLQ | 1 | Repackager or relabeler | accessdata.fda.gov |
| Knife, Ophthalmic | HNN | 1 | Repackager or relabeler | accessdata.fda.gov |
| Lacrimal Stents And Intubation Sets | OKS | U | Repackager or relabeler | accessdata.fda.gov |
| Laser, Ophthalmic | HQF | 2 | Repackager or relabeler | accessdata.fda.gov |
| Lens, Spectacle, Non-Custom (Prescription) | HQG | 1 | Repackager or relabeler | accessdata.fda.gov |
| Loop, Wire | JYQ | 1 | Repackager or relabeler | accessdata.fda.gov |
| Mallet, Surgical, General & Plastic Surgery | GFJ | 1 | Repackager or relabeler | accessdata.fda.gov |
| Marker, Ocular | HMR | 1 | Repackager or relabeler | accessdata.fda.gov |
| Mask, Scavenging | KHA | 1 | Repackager or relabeler | accessdata.fda.gov |
| Microscope, Operating & Accessories, Ac-Powered, Ophthalmic | HRM | 1 | Repackager or relabeler | accessdata.fda.gov |
| Microscope, Operating, Non-Electric, Ophthalmic | HRB | 1 | Repackager or relabeler | accessdata.fda.gov |
| Monitor, Eye Movement | HLL | 2 | Repackager or relabeler | accessdata.fda.gov |
| Needle, Ophthalmic Suturing | HNM | 1 | Repackager or relabeler | accessdata.fda.gov |
| Non-Surgical Gown | OEA | 1 | Repackager or relabeler | accessdata.fda.gov |
| Ophthalmoscope, Battery-Powered | HLJ | 2 | Repackager or relabeler | accessdata.fda.gov |
| Otoscope | ERA | 1 | Repackager or relabeler | accessdata.fda.gov |
| Perimeter, Automatic, Ac-Powered | HPT | 1 | Repackager or relabeler | accessdata.fda.gov |
| Plug, Punctum | LZU | U | Repackager or relabeler | accessdata.fda.gov |
| Probe, Lachrymal | HNL | 1 | Repackager or relabeler | accessdata.fda.gov |
| Probe, Trabeculotomy | HNK | 1 | Repackager or relabeler | accessdata.fda.gov |
| Projector, Ophthalmic | HOS | 1 | Repackager or relabeler | accessdata.fda.gov |
| Punch, Corneo-Scleral | HNJ | 1 | Repackager or relabeler | accessdata.fda.gov |
| Pupillometer, Manual | HLH | 1 | Repackager or relabeler | accessdata.fda.gov |
| Refractometer, Ophthalmic | HKO | 1 | Repackager or relabeler | accessdata.fda.gov |
| Refractor, Manual, Non-Powered, Including Phoropter | HKN | 1 | Repackager or relabeler | accessdata.fda.gov |
| Respirator, Surgical | MSH | 2 | Repackager or relabeler | accessdata.fda.gov |
| Retinoscope, Battery-Powered | HKM | 1 | Repackager or relabeler | accessdata.fda.gov |
| Retractor, Ophthalmic | HNI | 1 | Repackager or relabeler | accessdata.fda.gov |
| Ring, Ophthalmic (Flieringa) | HNH | 1 | Repackager or relabeler | accessdata.fda.gov |
| Rongeur, Lachrymal Sac | HNG | 1 | Repackager or relabeler | accessdata.fda.gov |
| Scissors, Ophthalmic | HNF | 1 | Repackager or relabeler | accessdata.fda.gov |
| Set, Lens, Trial, Ophthalmic | HPC | 1 | Repackager or relabeler | accessdata.fda.gov |
| Spatula, Ophthalmic | HND | 1 | Repackager or relabeler | accessdata.fda.gov |
| Spectacle, Magnifying | HOI | 1 | Repackager or relabeler | accessdata.fda.gov |
| Specula, Ophthalmic | HNC | 1 | Repackager or relabeler | accessdata.fda.gov |
| Spoon, Ophthalmic | HNB | 1 | Repackager or relabeler | accessdata.fda.gov |
| Spud, Ophthalmic | HNA | 1 | Repackager or relabeler | accessdata.fda.gov |
| Stand, Instrument, Ac-Powered, Ophthalmic | HMF | 1 | Repackager or relabeler | accessdata.fda.gov |
| Sunglasses (Non-Prescription Including Photosensitive) | HQY | 1 | Repackager or relabeler | accessdata.fda.gov |
| System, Imaging, Pulsed Echo, Ultrasonic | IYO | 2 | Repackager or relabeler | accessdata.fda.gov |
| Table, Instrument, Powered, Ophthalmic | HRJ | 1 | Repackager or relabeler | accessdata.fda.gov |
| Tester, Color Vision | HIT | 1 | Repackager or relabeler | accessdata.fda.gov |
| Thermometer, Clinical Color Change | FQZ | 1 | Repackager or relabeler | accessdata.fda.gov |
| Thermometer, Clinical Mercury | FLK | 2 | Repackager or relabeler | accessdata.fda.gov |
| Tonometer, Manual | HKY | 2 | Repackager or relabeler | accessdata.fda.gov |
| Transducer, Ultrasonic, Diagnostic | ITX | 2 | Repackager or relabeler | accessdata.fda.gov |
| Trephine, Manual, Ophthalmic | HRH | 1 | 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 |
|---|
| May 3, 2013 | K121243 | ULTRASONIC BIOMETER FOR OPHTHALMOLOGY ULTRASONIC PACHYMETER | IYO | Substantially Equivalent | MEDA Co., Ltd. | accessdata.fda.gov |
| August 9, 2012 | K121142 | CRAWFORD BIOCANALICULUS INTUBATION | OKS | Substantially Equivalent | Fci Sas (France Chirurgie Instrumentation) | accessdata.fda.gov |
| November 7, 2006 | K052599 | 66 VISION TECH OPHTHALMOSCOPE, MODELS YZ6E, YZ6F, YZ6G, YZ11, YZ11C, YZ11D, YZ25A | HLJ | Substantially Equivalent | Suzhou 66 Vision Tech Co., Ltd. | accessdata.fda.gov |
| July 11, 2006 | K061398 | SNUG PLUG PUNCTUM PLUG | LZU | Substantially Equivalent | Fci Ophthalmics, Inc. | accessdata.fda.gov |
| April 19, 2000 | K992294 | BIOCERAMIC ORBITAL IMPLANT | HPZ | Substantially Equivalent | Fci Ophthalmics, Inc. | accessdata.fda.gov |
| March 30, 1999 | K990075 | LPULSA SYL-9000 OPHTHALMIC YAG LASER | HQF | Substantially Equivalent | Light-Med(Usa), Inc. | accessdata.fda.gov |
| September 18, 1998 | K980816 | RETINAL DETACHMENT IMPLANTS, INCLUDING BANDS, STRIPS (RAILS) AND SPONGES | HQX | Substantially Equivalent | Fci Ophthalmics, Inc. | accessdata.fda.gov |
| May 8, 1995 | K945541 | SCHIOTZ TONOMETER SPEC. 5 STRAIGHT, INCLINED, 3INCLINED SCALE | HKY | Substantially Equivalent | Rudolf Riester GmbH & Co. KG | accessdata.fda.gov |
Compare with other makers
Updated May 3, 2013. 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.