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U.S. FDA Medical Device Tonsil Suturing Needle Requirements


FDA Medical Device Definition: An ear, nose, and throat manual surgical instrument is one of a variety of devices intended for use in surgical procedures to examine or treat the bronchus, esophagus, trachea, larynx, pharynx, nasal and paranasal sinus, or ear. This generic type of device includes the esophageal dilator; tracheal bistour (a long, narrow surgical knife); tracheal dilator; tracheal hook; laryngeal injection set; laryngeal knife; laryngeal saw; laryngeal trocar; laryngectomy tube; adenoid curette; adenotome; metal tongue depressor; mouth gag; oral screw; salpingeal curette; tonsillectome; tonsil guillotine; tonsil screw; tonsil snare; tonsil suction tube; tonsil suturing hook; antom reforator; ethmoid curette; frontal sinus-rasp; nasal curette; nasal rasp; nasal rongeur; nasal saw; nasal scissors; nasal snare; sinus irrigator; sinus trephine; ear curette; ear excavator; ear rasp; ear scissor, ear snare; ear spoon; ear suction tube; malleous ripper; mastoid gauge; microsurgical ear chisel; myringotomy tube inserter; ossici holding clamp; sacculotomy tack inserter; vein press; wire ear loop; microrule; mirror; mobilizer; ear, nose, and throat punch; ear, nose and throat knife; and ear, nose, and throat trocar.

Registrar Corp assists Tonsil Suturing Needle companies with:

  • FDA Tonsil Suturing Needle Establishment Registration
  • FDA Tonsil Suturing Needle Listing
  • FDA Tonsil Suturing Needle Label Requirements and Exceptions
  • FDA Tonsil Suturing Needle Import Information
  • FDA Tonsil Suturing Needle Detentions (Tonsil Suturing Needle Entry Refusals)
  • General U.S. Food and Drug Administration Medical Device Guidelines for:
       - Tonsil Suturing Needle Manufacturers (Tonsil Suturing Needle Suppliers)
       - Tonsil Suturing Needle Distributors
       - Tonsil Suturing Needle Processors
       - Tonsil Suturing Needle Repackers
       - Tonsil Suturing Needle Relabelers
       - Tonsil Suturing Needle Exporters
       - Tonsil Suturing Needle Importers
For more information about Tonsil Suturing Needle 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.
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