Data / Medical devices / Liechtenstein
Medical device makers in Liechtenstein: 10 FDA-registered establishments
10 establishments in Liechtenstein are registered with the FDA to make medical devices for the US market, listing 50 device types. 5 have a 510(k) clearance or PMA approval on file and 2 have a recall event. FDA data exported November 2, 2026.
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- LiechtensteinCountry
Device types made here
Device types with the most registered makers in this country.
| Device | Product code | Makers |
|---|---|---|
| Powder, Porcelain | EIH | 4 |
| Abutment, Implant, Dental, Endosseous | NHA | 1 |
| Accessories, Implant, Dental, Endosseous | NDP | 1 |
| Bur, Dental | EJL | 1 |
| Instrument, Diamond, Dental | DZP | 1 |
| Point, Abrasive | EHL | 1 |
| Syringe, Restorative And Impression Material | EID | 1 |
| Mouthpiece, Saliva Ejector | DYN | 1 |
| Instruments, Dental Hand | DZN | 1 |
| Accessories, Retractor, Dental | EIF | 1 |
| Adhesive, Denture, Polyvinyl Methylether Maleic Acid Calcium-Sodium Double Salt | KOO | 1 |
| Cleanser, Denture, Over The Counter | EFT | 1 |
| Dental Barriers And Sleeves | PEM | 1 |
| Tray, Impression, Preformed | EHY | 1 |
| Massager, Therapeutic, Electric | ISA | 1 |
| Bag, Reservoir | BTC | 1 |
| Light Based Over The Counter Wrinkle Reduction | OHS | 1 |
| Over-The-Counter Powered Light Based Laser For Acne | OLP | 1 |
| Stimulator, Muscle, Powered, For Muscle Conditioning | NGX | 1 |
| Pin, Retentive And Splinting, And Accessory Instruments | EBL | 1 |
| Drill, Dental, Intraoral | DZA | 1 |
| Cement, Dental | EMA | 1 |
| Crown And Bridge, Temporary, Resin | EBG | 1 |
| Material, Tooth Shade, Resin | EBF | 1 |
| Varnish, Cavity | LBH | 1 |
| Agent, Tooth Bonding, Resin | KLE | 1 |
| Resin, Denture, Relining, Repairing, Rebasing | EBI | 1 |
| Teeth, Porcelain | ELL | 1 |
| Sealant, Pit And Fissure, And Conditioner | EBC | 1 |
| Activator, Ultraviolet, For Polymerization | EBZ | 1 |
| Coating, Filling Material, Resin | EBD | 1 |
| Applicator, Resin | KXR | 1 |
| Agent, Polishing, Abrasive, Oral Cavity | EJR | 1 |
| Denture, Plastic, Teeth | ELM | 1 |
| Disk, Abrasive | EHJ | 1 |
| Material, Impression Tray, Resin | EBH | 1 |
| Orthosis, Limb Brace | IQI | 1 |
| Dental Abutment Design Software For Dental Laboratory | PNP | 1 |
| Alloy, Metal, Base | EJH | 1 |
| Articulators | EJP | 1 |
| Wheel, Polishing Agent | EJQ | 1 |
| Bandage, Liquid, Skin Protectant | NEC | 1 |
| Flowmeter, Calibration, Gas | BXY | 1 |
| Dam, Rubber | EIE | 1 |
| Facebow | KCR | 1 |
| Amalgamator, Dental, Ac-Powered | EFD | 1 |
| Ink, Arch Tracing | KZO | 1 |
| Carboxymethylcellulose Sodium Or Polyvinyl Methylether Maleic Acid Calcium-Sodium | KOT | 1 |
| Cushion, Denture, Over The Counter | EHS | 1 |
| Device, External Penile Rigidity | LKY | 1 |
Makers in Liechtenstein
Best documented first: most 510(k) clearances and PMA approvals.
| Maker | Location | Device types | 510(k) clearances | PMA approvals | Recall events | Source |
|---|---|---|---|---|---|---|
| Ivoclar Vivadent AG | Schaan, Liechtenstein | 32 | 74 | 0 | 2 | api.fda.gov |
| BEMER Int. AG | Triesen, Liechtenstein | 3 | 4 | 0 | 1 | api.fda.gov |
| Estetic Ceram AG | Triesen, Liechtenstein | 1 | 2 | 0 | 0 | api.fda.gov |
| Bonyf AG | Vaduz, Liechtenstein | 5 | 1 | 0 | 0 | api.fda.gov |
| Wohlwend AG | Schellenberg, Liechtenstein | 1 | 1 | 0 | 0 | api.fda.gov |
| Centropix Global AG | Ruggell, Liechtenstein | 1 | 0 | 0 | 0 | api.fda.gov |
| Chemichl AG | Vaduz, Liechtenstein | 1 | 0 | 0 | 0 | api.fda.gov |
| Edenta Etablissement | SCHAANWALD Mauren, Liechtenstein | 6 | 0 | 0 | 0 | api.fda.gov |
| Fma Mechatronic Solutions AG | Schaan, Liechtenstein | 2 | 0 | 0 | 0 | api.fda.gov |
| Swiss Cupping AG | Vaduz, Liechtenstein | 2 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. 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.