Suture Retention Device Suppliers
Aesculap Ag | Address: 1120, Tuttlingen, Donau D-78532, Germany 
www.aesculap.de | Send Inquiry | Phone: +94-(610)-9849074
FDA Registration: 9610612
Products: Vaginal Retractors (FDA Code: HDL), Forceps (FDA Code: HTD), Probes (FDA Code: HXB), Saws (FDA Code: HSO), Gastroenterologic Needle Holder (FDA Code: FHQ), Self-Retaining Retractors (FDA Code: FFO), ...
Aesculap Ag offers instruments for minimal invasive surgery. Our product range includes surgical instruments for open or minimally invasive approaches, implants for orthopedic, neuro and spinal surger more...
www.aesculap.de | Send Inquiry | Phone: +94-(610)-9849074
FDA Registration: 9610612
Products: Vaginal Retractors (FDA Code: HDL), Forceps (FDA Code: HTD), Probes (FDA Code: HXB), Saws (FDA Code: HSO), Gastroenterologic Needle Holder (FDA Code: FHQ), Self-Retaining Retractors (FDA Code: FFO), ...
Aesculap Ag offers instruments for minimal invasive surgery. Our product range includes surgical instruments for open or minimally invasive approaches, implants for orthopedic, neuro and spinal surger more...
HGR Instrumente GmbH | Address: Sattlerstr. 19, Tuttlingen- Nendingen 78532, Germany
www.hgr-instrumente.de | Phone: +49-(7461)-78672
FDA Registration: 8044098 Year Established: 1992 Quality: DIN EN ISO 13485 : 2003. Certified
Products: Saws (FDA Code: HSO), Lacrimal Probes (FDA Code: HNL), Mini-Lacrimal Probes, Disposable Ear Curette, Child Ear Curette, Round Ear Curette, ...
HGR Instrumente GmbH offers eye, ENT & arthroscopy instruments, self-retaining retractors, bone spoons, chisels and rasps. more...
www.hgr-instrumente.de | Phone: +49-(7461)-78672
FDA Registration: 8044098 Year Established: 1992 Quality: DIN EN ISO 13485 : 2003. Certified
Products: Saws (FDA Code: HSO), Lacrimal Probes (FDA Code: HNL), Mini-Lacrimal Probes, Disposable Ear Curette, Child Ear Curette, Round Ear Curette, ...
HGR Instrumente GmbH offers eye, ENT & arthroscopy instruments, self-retaining retractors, bone spoons, chisels and rasps. more...
Davis And Geck Caribe, Ltd. | Address: Zona Franca De San Isidro, Carretara San Isidro Km 17, Santo Domingo, Dominican Republic
Phone: 203-845-1000
FDA Registration: 9612501
Products: Oxygen Masks (FDA Code: BYG), Forceps (FDA Code: HTD), Catheter Introducers (FDA Code: DYB), Arthroscopes (FDA Code: HRX), Catheter Stylets (FDA Code: DRB), Electrode Cables (FDA Code: IKD), ...
Davis And Geck Caribe, Ltd. specializes in the production of polytetrafluorethylene pledget, disposable endoscopic specimen pouch, steel sutures and umbilical tape-sterile round cotton tape. more...
Phone: 203-845-1000
FDA Registration: 9612501
Products: Oxygen Masks (FDA Code: BYG), Forceps (FDA Code: HTD), Catheter Introducers (FDA Code: DYB), Arthroscopes (FDA Code: HRX), Catheter Stylets (FDA Code: DRB), Electrode Cables (FDA Code: IKD), ...
Davis And Geck Caribe, Ltd. specializes in the production of polytetrafluorethylene pledget, disposable endoscopic specimen pouch, steel sutures and umbilical tape-sterile round cotton tape. more...
Canica Design Inc. | Address: 36 Mill Street, Almonte, Ontario K0A 1A0, Canada 
www.canica.com | Send Inquiry | Phone: +1-(613)-256-0350, 800-705-8312
Year Established: 1998
Products: Scalpel Handle (FDA Code: GDZ), Blood Collection Lancet (FDA Code: FMK), General Surgical Manual Instrument (FDA Code: MDM), One-Piece Scalpel (FDA Code: GDX), Removable Skin Clip (FDA Code: FZQ), Skin Closure System (FDA Code: MKY), ...
Canica Design Inc. is a medical device company that specializes in designing devices for the mechanical manipulation of soft tissues for use in acute care and chronic care settings. We develop a wide more...
www.canica.com | Send Inquiry | Phone: +1-(613)-256-0350, 800-705-8312
Year Established: 1998
Products: Scalpel Handle (FDA Code: GDZ), Blood Collection Lancet (FDA Code: FMK), General Surgical Manual Instrument (FDA Code: MDM), One-Piece Scalpel (FDA Code: GDX), Removable Skin Clip (FDA Code: FZQ), Skin Closure System (FDA Code: MKY), ...
Canica Design Inc. is a medical device company that specializes in designing devices for the mechanical manipulation of soft tissues for use in acute care and chronic care settings. We develop a wide more...
FDA Code / Regulation: KGS / 878.4930
A suture retention device is a device, such as a retention bridge, a surgical button, or a suture bolster, intended to aid wound healing by distributing suture tension over a larger area in the patient.
Classification. Class I (general controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter, subject to the limitations in 878.9.
