Skeletal Kinetics LLC
United StatesFDA applicant, unverified
- Devices
- 119
- FDA recalls
- 49
What Skeletal Kinetics LLC makes
Skeletal Kinetics LLC manufactures bone void fillers and related orthopedic devices designed to support bone regeneration and structural integrity. Their portfolio includes injectable and scaffold-based fillers, such as calcium phosphate granules and porous bone substitutes, as well as specialized implants like the OsteoVation Impact system for fracture stabilization. These products are tailored for use in trauma, spinal, and craniomaxillofacial (CMF) applications, addressing defects and voids in bone tissue.
The company’s devices are classified under FDA categories, including Class II and Unclassified (U), with many authorised via the 510(k) pathway. Products are listed in the FDA’s 510(k) registry, reflecting their regulatory compliance in the United States. The manufacturer operates from its base in the US, adhering to applicable medical device regulations
Catalogue
Search and filter all 119 devicesShowing 101-119 of 119
Company details
- DUNS number
- 140071411
- [email protected]
- Phone
- +1(408)366-5014
FDA recalls
FDA recall records list 49 recalls initiated by SKELETAL KINETICS LLC, the earliest on 2015-05-29 and the most recent on 2020-04-06. By recorded status: 49 terminated. The reasons filed fall into these groups: labeling or instructions for use, sterility or contamination and packaging. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.
Recalls initiated per year
- 2017 0
- 2018 0
- 2019 2
- 2020 46
- 2021 0
- 2022 0
- 2023 0
- 2024 0
- 2025 0
- 2026 0
2020
- 6 Apr 2020 Z-2592-2020 Class II Terminated Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include incomplete bone formation or lack of bone formation, delayed union, or nonunion.
Full distribution text
- 6 Apr 2020 Z-2593-2020 Class II Terminated Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include incomplete bone formation or lack of bone formation, delayed union, or nonunion.
Full distribution text
- 6 Apr 2020 Z-2594-2020 Class II Terminated Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include incomplete bone formation or lack of bone formation, delayed union, or nonunion.
Full distribution text
- 6 Apr 2020 Z-2595-2020 Class II Terminated Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include incomplete bone formation or lack of bone formation, delayed union, or nonunion.
Full distribution text
- 6 Apr 2020 Z-2596-2020 Class II Terminated Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include incomplete bone formation or lack of bone formation, delayed union, or nonunion.
Full distribution text
- 6 Apr 2020 Z-2597-2020 Class II Terminated Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include incomplete bone formation or lack of bone formation, delayed union, or nonunion.
Full distribution text
- 6 Apr 2020 Z-2598-2020 Class II Terminated Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include incomplete bone formation or lack of bone formation, delayed union, or nonunion.
Full distribution text
- 6 Apr 2020 Z-2599-2020 Class II Terminated Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include incomplete bone formation or lack of bone formation, delayed union, or nonunion.
Full distribution text
- 6 Apr 2020 Z-2600-2020 Class II Terminated Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include incomplete bone formation or lack of bone formation, delayed union, or nonunion.
Full distribution text
- 6 Apr 2020 Z-2601-2020 Class II Terminated Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include incomplete bone formation or lack of bone formation, delayed union, or nonunion.
Full distribution text
- 6 Apr 2020 Z-2592-2020 Class II Terminated Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include incomplete bone formation or lack of bone formation, delayed union, or nonunion.
Show the 25 most recent of 49 recalls
2020
- 6 Apr 2020 Z-2602-2020 Class II Terminated Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include incomplete bone formation or lack of bone formation, delayed union, or nonunion.
Full distribution text
- 6 Apr 2020 Z-2603-2020 Class II Terminated Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include incomplete bone formation or lack of bone formation, delayed union, or nonunion.
Full distribution text
- 6 Apr 2020 Z-2604-2020 Class II Terminated Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include incomplete bone formation or lack of bone formation, delayed union, or nonunion.
Full distribution text
- 6 Apr 2020 Z-2605-2020 Class II Terminated Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include incomplete bone formation or lack of bone formation, delayed union, or nonunion.
Full distribution text
- 6 Apr 2020 Z-2606-2020 Class II Terminated Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include incomplete bone formation or lack of bone formation, delayed union, or nonunion.
Full distribution text
- 6 Apr 2020 Z-2607-2020 Class II Terminated Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include incomplete bone formation or lack of bone formation, delayed union, or nonunion.
Full distribution text
- 6 Apr 2020 Z-2608-2020 Class II Terminated Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include incomplete bone formation or lack of bone formation, delayed union, or nonunion.
Full distribution text
- 6 Apr 2020 Z-2609-2020 Class II Terminated Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include incomplete bone formation or lack of bone formation, delayed union, or nonunion.
Full distribution text
- 6 Apr 2020 Z-2610-2020 Class II Terminated Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include incomplete bone formation or lack of bone formation, delayed union, or nonunion.
Full distribution text
- 6 Apr 2020 Z-2611-2020 Class II Terminated Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include incomplete bone formation or lack of bone formation, delayed union, or nonunion.
Full distribution text
- 6 Apr 2020 Z-2612-2020 Class II Terminated Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include incomplete bone formation or lack of bone formation, delayed union, or nonunion.
Full distribution text
- 6 Apr 2020 Z-2613-2020 Class II Terminated Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include incomplete bone formation or lack of bone formation, delayed union, or nonunion.
Full distribution text
- 6 Apr 2020 Z-2614-2020 Class II Terminated Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include incomplete bone formation or lack of bone formation, delayed union, or nonunion.
Full distribution text
- 6 Apr 2020 Z-2615-2020 Class II Terminated Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include incomplete bone formation or lack of bone formation, delayed union, or nonunion.
Full distribution text
- 6 Apr 2020 Z-2616-2020 Class II Terminated Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include incomplete bone formation or lack of bone formation, delayed union, or nonunion.
Full distribution text
- 6 Apr 2020 Z-2602-2020 Class II Terminated Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include incomplete bone formation or lack of bone formation, delayed union, or nonunion.