Data / Medical devices / United Kingdom / Bailey Instruments Ltd
Bailey Instruments Ltd: FDA-registered device maker in Manchester, United Kingdom, 1 510(k) clearance
Bailey Instruments Ltd is registered with the FDA (registration 3001084743) in Manchester, United Kingdom. It lists 54 device types. The FDA files 1 510(k) clearance under its listings, the newest dated November 30, 2017. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3001084743
- Address
- Unit 19 Guinness Road Trading Estate Trafford Park, Manchester, United Kingdom, M17 1SB
- Owner or operator
- Bailey Instruments Ltd (9033619)
- Roles
- Manufacturer
- First device listed
- April 21, 1998
- Registered through
- 2026
- Brand names listed
- INSTRUMENT, MANUAL, SURGICAL, GENERAL USE
Devices it lists
| Device | Product code | Class | Role | Source |
|---|
| Bur, Surgical, General & Plastic Surgery | GFF | 1 | Manufacturer | accessdata.fda.gov |
| Continuous Measurement Thermometer | FLL | 2 | Manufacturer | accessdata.fda.gov |
| Curette, Surgical, General Use | FZS | 1 | Manufacturer | accessdata.fda.gov |
| Cutter, Surgical | FZT | 1 | Manufacturer | accessdata.fda.gov |
| Cutter, Wire | HXZ | 1 | Manufacturer | accessdata.fda.gov |
| Depressor, Tongue, Non-Surgical | FMA | 1 | Manufacturer | accessdata.fda.gov |
| Dilator, Cervical, Fixed Size | HDQ | 1 | Manufacturer | accessdata.fda.gov |
| Dilator, Tracheal | KCG | 1 | Manufacturer | accessdata.fda.gov |
| Discriminator, Two-Point | GWI | 1 | Manufacturer | accessdata.fda.gov |
| Dissector, Surgical, General & Plastic Surgery | GDI | 1 | Manufacturer | accessdata.fda.gov |
| Ear, Nose, And Throat Surgical Tray | OGR | 1 | Manufacturer | accessdata.fda.gov |
| Elevator, Surgical, General & Plastic Surgery | GEG | 1 | Manufacturer | accessdata.fda.gov |
| Esthesiometer | GXB | 1 | Manufacturer | accessdata.fda.gov |
| Forceps, Biopsy, Gynecological | HFB | 1 | Manufacturer | accessdata.fda.gov |
| Forceps, Ent | KAE | 1 | Manufacturer | accessdata.fda.gov |
| Forceps, General & Plastic Surgery | GEN | 1 | Manufacturer | accessdata.fda.gov |
| Forceps, Wire Holding | HYA | 1 | Manufacturer | accessdata.fda.gov |
| Fork, Tuning | GWX | 1 | Manufacturer | accessdata.fda.gov |
| Handle, Instrument, Dental | EJB | 1 | Manufacturer | accessdata.fda.gov |
| Handle, Scalpel | GDZ | 1 | Manufacturer | accessdata.fda.gov |
| Hook, Surgical, General & Plastic Surgery | GDG | 1 | Manufacturer | accessdata.fda.gov |
| Insoles, Medical | KYS | 1 | Manufacturer | accessdata.fda.gov |
| Instrument, Cutting, Orthopedic | HTZ | 1 | Manufacturer | accessdata.fda.gov |
| Instrument, Ent Manual Surgical | LRC | 1 | Manufacturer | accessdata.fda.gov |
| Instrument, Manual, Surgical, General Use | MDM | 1 | Manufacturer | accessdata.fda.gov |
| Kit, Surgical Instrument, Disposable | KDD | 1 | Manufacturer | accessdata.fda.gov |
| Knife, Ent | KTG | 1 | Manufacturer | accessdata.fda.gov |
| Mallet, Surgical, General & Plastic Surgery | GFJ | 1 | Manufacturer | accessdata.fda.gov |
| Maternity Kit | PVT | 1 | Manufacturer | accessdata.fda.gov |
| Mirror, Ent | KAI | 1 | Manufacturer | accessdata.fda.gov |
| Orthopedic Manual Surgical Instrument | LXH | 1 | Manufacturer | accessdata.fda.gov |
| Orthosis, Corrective Shoe | KNP | 1 | Manufacturer | accessdata.fda.gov |
| Percussor | GWZ | 1 | Manufacturer | accessdata.fda.gov |
| Probe, Ent | KAK | 1 | Manufacturer | accessdata.fda.gov |
| Rasp | HTR | 1 | Manufacturer | accessdata.fda.gov |
| Rasp, Surgical, General & Plastic Surgery | GAC | 1 | Manufacturer | accessdata.fda.gov |
| Retractor | GAD | 1 | Manufacturer | accessdata.fda.gov |
| Ring Cutter | FNS | 1 | Manufacturer | accessdata.fda.gov |
| Rongeur | HTX | 1 | Manufacturer | accessdata.fda.gov |
| Scissors, General, Surgical | LRW | 1 | Manufacturer | accessdata.fda.gov |
| Scissors, Medical, Disposable | JOK | 1 | Manufacturer | accessdata.fda.gov |
| Scissors, Umbilical | HDJ | 1 | Manufacturer | accessdata.fda.gov |
| Single Use Instrument Tray | OJV | 1 | Manufacturer | accessdata.fda.gov |
| Sound, Uterine | HHM | 1 | Manufacturer | accessdata.fda.gov |
| Spatula, Surgical, General & Plastic Surgery | GAF | 1 | Manufacturer | accessdata.fda.gov |
| Speculum, Ent | EPY | 1 | Manufacturer | accessdata.fda.gov |
| Speculum, Vaginal, Metal | HDF | 1 | Manufacturer | accessdata.fda.gov |
| Suture Kit | OVN | 2 | Manufacturer | accessdata.fda.gov |
| Suture Removal Kit | MCZ | 1 | Manufacturer | accessdata.fda.gov |
| Syringe, Cartridge | EJI | 2 | Manufacturer | accessdata.fda.gov |
| Tourniquet, Nonpneumatic | GAX | 1 | Manufacturer | accessdata.fda.gov |
| Tray, Surgical | LRP | 1 | Manufacturer | accessdata.fda.gov |
| Tube, Ear Suction | JZF | 1 | Manufacturer | accessdata.fda.gov |
| Wound Dressing Kit | MCY | 2 | Manufacturer | 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 |
|---|
| November 30, 2017 | K171578 | Infrared thermometer | FLL | Substantially Equivalent | Shenzhen Aeon Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated November 30, 2017. 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.