U.S. FDA Medical Device Orbital Compressor Requirements
FDA Medical Device Definition: A manual ophthalmic surgical instrument is a nonpowered, handheld device intended to aid or perform ophthalmic surgical procedures. This generic type of device includes the manual corneal burr, ophthalmic caliper, ophthalmic cannula, eyelid clamp, ophthalmic muscle clamp, iris retractor clip, orbital compressor, ophthalmic curette, cystotome, orbital depressor, lachrymal dilator, erisophake, expressor, ophthalmic forcep, ophthalmic hook, sphere introducer, ophthalmic knife, ophthalmic suturing needle, lachrymal probe, trabeculotomy probe, cornea-sclera punch, ophthalmic retractor, ophthalmic ring (Flieringa), lachrymal sac rongeur, ophthalmic scissors, enucleating snare, ophthalmic spatula, ophthalmic specula, ophthalmic spoon, ophthalmic spud, trabeculotome or ophthalmic manual trephine.
Registrar Corp assists Orbital Compressor companies with:
FDA Orbital Compressor Establishment Registration
FDA Orbital Compressor Listing
FDA Orbital Compressor Label Requirements and Exceptions
FDA Orbital Compressor Import Information
FDA Orbital Compressor Detentions (Orbital Compressor Entry Refusals)
General U.S. Food and Drug Administration Medical Device Guidelines for:
- Orbital Compressor Manufacturers (Orbital Compressor Suppliers)
- Orbital Compressor Distributors
- Orbital Compressor Processors
- Orbital Compressor Repackers
- Orbital Compressor Relabelers
- Orbital Compressor Exporters
- Orbital Compressor Importers
For more information about Orbital Compressor Medical Devices, simply click below:
U.S. FDA Regulations:
U.S. FDA 510(k) Regulation: 21 C.F.R. section 814.9.
Registrar Corp assists businesses with U.S. FDA compliance. Certificates of Registration issued by Registrar Corp provide confirmation to industry that you are fulfilling U.S. FDA registration requirements. U.S. FDA does not issue or recognize Certificates of Registration. Registrar Corp is not affiliated with the U.S. Food and Drug Administration.