Skeletal Kinetics LLC
United StatesFDA applicant, unverified
- Devices
- 119
- FDA recalls
- 49
At a glance
Market reach
- United States
- FDA recalls
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 1-50 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.
Frequently asked questions
How many devices does SKELETAL KINETICS LLC have in the registry?
The registry currently lists 119 devices for SKELETAL KINETICS LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list SKELETAL KINETICS LLC's devices?
Among its 50 most recently registered devices, SKELETAL KINETICS LLC has devices listed in FDA GUDID (50 devices).
What risk classes do SKELETAL KINETICS LLC's devices fall under?
Among its 50 most recently registered devices, the classes recorded for SKELETAL KINETICS LLC's devices are Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for SKELETAL KINETICS LLC?
FDA recall records list 49 recalls initiated by SKELETAL KINETICS LLC, the most recent initiated on 6 Apr 2020. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.
What are the newest devices from SKELETAL KINETICS LLC in the registry?
The most recently registered devices listed for SKELETAL KINETICS LLC include OsteoMed 390-6005, OsteoVation 390-4202, OsteoVation 390-6002 and SKaffold SKMX-FL05.