Seare Biomedical Corp.
United StatesFDA applicant, unverified
- Devices
- 8
What Seare Biomedical Corp. makes
Seare Biomedical Corp. manufactures silicone-based medical devices including tissue expanders, sheeting, nasal implants, blocks, malar implants, chin implants, pectoralis implants, and silicone rods.
The company's products are listed in the FDA 510(k) registry and are classified as Class II and Class U devices. Seare Biomedical Corp. is based in the US.
Catalogue
Seare Biomedical Silicone Tissue Expander Ref K983792
Regimes: 510(k) Registry: 510(k)Seare Biomedical Silicone Sheeting Ref K983041
Regimes: 510(k) Registry: 510(k)Seare Biomedical Nasal Implants Ref K982753
Regimes: 510(k) Registry: 510(k)Seare Biomedical Silicone Block Ref K983043
Regimes: 510(k) Registry: 510(k)Seare Biomedical Malar Implants Ref K982763
Regimes: 510(k) Registry: 510(k)Seare Biomedical Chin Implants Ref K982752
Regimes: 510(k) Registry: 510(k)Seare Biomedical Pectoralis Implant Ref K982762
Regimes: 510(k) Registry: 510(k)Seare Biomedical Silicone Rods Ref K983630
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Seare Biomedical Corp. have in the registry?
The registry currently lists 8 devices for Seare Biomedical Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Seare Biomedical Corp.'s devices?
Among its 8 most recently registered devices, Seare Biomedical Corp. has devices listed in FDA 510(k) (8 devices).
What risk classes do Seare Biomedical Corp.'s devices fall under?
Among its 8 most recently registered devices, the classes recorded for Seare Biomedical Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Seare Biomedical Corp. in the registry?
The most recently registered devices listed for Seare Biomedical Corp. include SEARE BIOMEDICAL SILICONE TISSUE EXPANDER, SEARE BIOMEDICAL SILICONE SHEETING, SEARE BIOMEDICAL NASAL IMPLANTS and SEARE BIOMEDICAL SILICONE BLOCK.