510(k) · Cleared
Recalled · Class II · 2025Optima Coil System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Balt USA, LLC · HCG Device, Neurovascular Embolization
Cleared on Feb 1, 2020 as substantially equivalent to K172390 (Blockade Medical, LLC (D.B.A. Balt Usa), 2018) after a 25-day review. Its family tree reaches back 23 generations to 1995. 6 later devices descend from it. It has been recalled 5 times.
- Decided
- Feb 1, 2020
- Review
- 25 days
- Class
- Class II
- Product code
- HCG
- Recalls
- 5
- Predicates
- 1
Its longest line of descent runs back 23 generations to K951256 (1995). 65 ancestors in all, the oldest K860840 (1986). 6 later devices descend from it, 2 citing it directly.
- Root · 23 generations backK951256 Detachable Platinum Coil (Guglielmi Detachable Coil, GDC)Target Therapeutics · 1995
- 19 generations between
- 3 generations backK142513 Barricade Embolization Coil SystemBlockade Medical · 2014
- 2 generations backK151760 Barricade Embolization Coil SystemBlockade Medical · 2015
- 1 generation backK172390 Optima Coil SystemBlockade Medical, LLC (D.B.A. Balt Usa) · 2018 · Recalled
- This deviceK200030 Optima Coil SystemBalt USA, LLC · 2020
- Descendant · cites it directly · 3 of its ownK223386 Optima Coil SystemBalt USA, LLC · 2022 · Recalled
- Descendant · 2 generations on · 2 of its ownK242582 Optima Coil System (OptiBlock Line Extension)Balt USA, LLC · 2024
- Descendant · 3 generations on · 1 of its ownK252700 Optima Coil System (Optima Packing Coil System)Balt USA, LLC · 2025
- Descendant · cites it directly · 1 of its ownK220699 Prestige Coil SystemBait USA, LLC · 2022 · Recalled
- Descendant · 4 generations on · 0 of its ownK254221 Optima Coil System (OptiOne Coil System)Balt USA, LLC · 2026
Show all 23 generations
- Root · 23 generations backK951256 Detachable Platinum Coil (Guglielmi Detachable Coil, GDC)Target Therapeutics · 1995
- 22 generations backK960705 Guglielmi Detachable CoilTarget Therapeutics · 1996
- 21 generations backK962503 Guglielmi Detachable CoilTarget Therapeutics · 1996
- 20 generations backK971395 Guglielmi Detachable Coil (GDC), Fibered Platinum Coil, .035 Type…Target Therapeutics · 1997
- 19 generations backK991139 Guglielmi Detachable (GDC)Boston Scientific, Target · 1999
- 18 generations backK012145 Microplex Coil SystemMicroVention, Inc. · 2001
- 17 generations backK020434 Microplex Coil System (MCS)MicroVention, Inc. · 2002
- 16 generations backK032590 Microplex Coil System (MCS), Hydrocoil Embolic System (Hes)MicroVention, Inc. · 2003
- 15 generations backK033836 Hydrocoil Embolic System (Hes)MicroVention, Inc. · 2003
- 14 generations backK041551 Modification to: Hydrocoil Embolic System (Hes)MicroVention, Inc. · 2004
- 13 generations backK050954 Microplex Coil System (MCS) and Hydrocoil Embolic System (Hes)MicroVention, Inc. · 2005 · Recalled
- 12 generations backK070656 Hydrocoil Embolic System (Hes)MicroVention, Inc. · 2007
- 11 generations backK080666 Hydrosoft and Hydrosoft Plus Embolization Coil SystemsMicroVention, Inc. · 2008
- 10 generations backK112226 Hydrocoil Embolic System (Hes)MicroVention, Inc. · 2011
- 9 generations backK113457 Hydrocoil Embolic System (Hes)MicroVention, Inc. · 2011
- 8 generations backK120908 Hydrocoil Embolic System (Hes)MicroVention, Inc. · 2012
- 7 generations backK123338 Barricade Embolization Coil SystemBlockade Medical · 2013
- 6 generations backK131475 Barricade Embolization Coil SystemBlockade Medical · 2013
- 5 generations backK132482 Barricade Embolization Coil SystemBlockade Medical · 2013
- 4 generations backK140104 Barricade Embolization Coil SystemBlockade Medical · 2014
- 3 generations backK142513 Barricade Embolization Coil SystemBlockade Medical · 2014
- 2 generations backK151760 Barricade Embolization Coil SystemBlockade Medical · 2015
- 1 generation backK172390 Optima Coil SystemBlockade Medical, LLC (D.B.A. Balt Usa) · 2018 · Recalled
- This deviceK200030 Optima Coil SystemBalt USA, LLC · 2020
Showing 5 of 6 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 6 · See all- K223386Optima Coil SystemBalt USA, LLC · 2022 · cites it directly3descendants
- K242582Optima Coil System (OptiBlock Line Extension)Balt USA, LLC · 2024 · 2 generations on2descendants
- K252700Optima Coil System (Optima Packing Coil System)Balt USA, LLC · 2025 · 3 generations on1descendant
- K220699Prestige Coil SystemBait USA, LLC · 2022 · cites it directly1descendant
- K254221Optima Coil System (OptiOne Coil System)Balt USA, LLC · 2026 · 4 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −23 | K951256 | Detachable Platinum Coil (Guglielmi Detachable Coil, GDC) | Target Therapeutics | 1995 | — |
| −22 | K960705 | Guglielmi Detachable Coil | Target Therapeutics | 1996 | — |
| −21 | K962503 | Guglielmi Detachable Coil | Target Therapeutics | 1996 | — |
| −20 | K971395 | Guglielmi Detachable Coil (GDC), Fibered Platinum Coil, .035 Type, Berenstein… | Target Therapeutics | 1997 | — |
| −19 | K991139 | Guglielmi Detachable (GDC) | Boston Scientific, Target | 1999 | — |
| −18 | K012145 | Microplex Coil System | MicroVention, Inc. | 2001 | — |
| −17 | K020434 | Microplex Coil System (MCS) | MicroVention, Inc. | 2002 | — |
| −16 | K032590 | Microplex Coil System (MCS), Hydrocoil Embolic System (Hes) | MicroVention, Inc. | 2003 | — |
| −15 | K033836 | Hydrocoil Embolic System (Hes) | MicroVention, Inc. | 2003 | — |
| −14 | K041551 | Modification to: Hydrocoil Embolic System (Hes) | MicroVention, Inc. | 2004 | — |
| −13 | K050954 | Microplex Coil System (MCS) and Hydrocoil Embolic System (Hes) | MicroVention, Inc. | 2005 | 16 |
| −12 | K070656 | Hydrocoil Embolic System (Hes) | MicroVention, Inc. | 2007 | — |
| −11 | K080666 | Hydrosoft and Hydrosoft Plus Embolization Coil Systems | MicroVention, Inc. | 2008 | — |
| −10 | K112226 | Hydrocoil Embolic System (Hes) | MicroVention, Inc. | 2011 | — |
| −9 | K113457 | Hydrocoil Embolic System (Hes) | MicroVention, Inc. | 2011 | — |
| −8 | K120908 | Hydrocoil Embolic System (Hes) | MicroVention, Inc. | 2012 | — |
| −7 | K123338 | Barricade Embolization Coil System | Blockade Medical | 2013 | — |
| −6 | K131475 | Barricade Embolization Coil System | Blockade Medical | 2013 | — |
| −5 | K132482 | Barricade Embolization Coil System | Blockade Medical | 2013 | — |
| −4 | K140104 | Barricade Embolization Coil System | Blockade Medical | 2014 | — |
| −3 | K142513 | Barricade Embolization Coil System | Blockade Medical | 2014 | — |
| −2 | K151760 | Barricade Embolization Coil System | Blockade Medical | 2015 | — |
| −1 | K172390 | Optima Coil System | Blockade Medical, LLC (D.B.A. Balt Usa) | 2018 | 4 |
| 0 (this device) | K200030 | Optima Coil System | Balt USA, LLC | 2020 | — |
| +1 | K223386 | Optima Coil System | Balt USA, LLC | 2022 | 1 |
| +2 | K242582 | Optima Coil System (OptiBlock Line Extension) | Balt USA, LLC | 2024 | — |
| +3 | K252700 | Optima Coil System (Optima Packing Coil System) | Balt USA, LLC | 2025 | — |
| +1 | K220699 | Prestige Coil System | Bait USA, LLC | 2022 | 2 |
| +4 | K254221 | Optima Coil System (OptiOne Coil System) | Balt USA, LLC | 2026 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1986 | 1 | 0 |
| 1988 | 3 | 0 |
| 1989 | 1 | 0 |
| 1990 | 1 | 0 |
| 1991 | 2 | 0 |
| 1992 | 5 | 0 |
| 1994 | 3 | 0 |
| 1995 | 2 | 0 |
| 1996 | 2 | 0 |
| 1997 | 1 | 0 |
| 2000 | 5 | 0 |
| 2001 | 1 | 0 |
| 2002 | 3 | 0 |
| 2003 | 4 | 0 |
| 2004 | 1 | 0 |
| 2005 | 1 | 0 |
| 2008 | 1 | 0 |
| 2009 | 2 | 0 |
| 2010 | 2 | 0 |
| 2011 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2022 | 2 | 0 |
| 2024 | 1 | 0 |
| 2025 | 2 | 0 |
| 2026 | 1 | 0 |
Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in HCG? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
Top candidate predicates for a new HCG device
- #1 K252700 Optima Coil System (Optima Packing Coil System)score 20.6 · 26 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (1)
Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K172390 | Optima Coil SystemSummary page 4…lass II, 21 CFR 882.5950 (HCG) CLASSIFICATION: Class II, 21 CFR 870.3300 (KRD) PRODUCT CODE: HCG, KRD PREDICATE Optima Coil System (K172390) DEVICE: PURPOSE OF The purpose of this Special 510(k) submission is to obtain market SUBMISSION: c… | 2018 |
What descends from it? (6)
2 later devices cite it directly; ranked here by how many devices descend from each in turn.
Has anything in its family been recalled? (0 Class I)
Recalls of this device
| Date | Class | Recall | Root cause | Reason |
|---|---|---|---|---|
| May 8, 2025 | Class II | Z-1988-2025 | Vendor change control | Due to radiopaque (RO) marker was not visible during angiography and it was determined that the RO marker was not manufactured to specification. |
| Jan 3, 2024 | Class II | Z-1041-2024 | Material/Component Contamination | Discoloration was identified along the delivery pusher which was attributed to corrosion of the hypotube. The material which caused the corrosion was identified as remnants of solder flux residue remaining on the hypotube component of the… |
| Sep 7, 2022 | Class II | Z-0103-2023 | Error in labeling | Product pouch label does not match up with carton label |
| Jul 26, 2022 | Class II | Z-1680-2022 | Under Investigation by firm | Products were released to customers prior to the approval and release of a test report authorizing the use of an existing material from an alternate supplier. |
| Jan 4, 2022 | Class II | Z-0660-2022 | Process control | Due to Label/Pouch mix-up. Pouches incorrectly labeled. Incorrect shelf carton label or pouch label due to inadequate manufacturing line clearance. As a result of this labeling mix-up, there is the possibility of inadvertently selecting… |
No ancestor or descendant has a Class I recall.
What does this lineage say?
- The line of descent spans 25 years and passes through 6 companies; a new generation was cleared every 9 months on median.
- 14 of the 65 ancestors have a recall of any class.
- Of its descendants, K223386 (Balt USA, LLC, 2022) has gone furthest, with 3 descendants of its own.
How does its category compare?
All HCG devicesHCG Device, Neurovascular Embolization: FDA decisions, review times, recalls and adverse event reports over 20 years. 2020, this device’s year, is highlighted.
FDA decisions per year · HCG
3in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · HCG
107in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · HCG
1in 2025
Class I (1 since 2007) Class II/III not classified
Adverse event reports per year · HCG
537in 2025
MAUDE reports naming product code HCG, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 8 | 50 | 1 | 326 |
| 2008 | 9 | 71 | 3 | 730 |
| 2009 | 7 | 48 | 0 | 821 |
| 2010 | 8 | 72 | 2 | 851 |
| 2011 | 9 | 78 | 1 | 894 |
| 2012 | 7 | 30 | 0 | 1,146 |
| 2013 | 7 | 67 | 2 | 1,103 |
| 2014 | 5 | 66 | 4 | 1,729 |
| 2015 | 5 | 60 | 0 | 1,598 |
| 2016 | 7 | 37 | 0 | 1,991 |
| 2017 | 5 | 97 | 0 | 2,494 |
| 2018 | 4 | 173 | 0 | 2,058 |
| 2019 | 1 | — | 0 | 1,763 |
| 2020 | 2 | — | 0 | 1,754 |
| 2021 | 5 | 103 | 0 | 2,268 |
| 2022 | 3 | 114 | 2 | 663 |
| 2023 | 2 | — | 0 | 568 |
| 2024 | 4 | 49 | 1 | 552 |
| 2025 | 3 | 107 | 1 (1) | 537 |
| 2026 | 4 | 30 | 1 | — |
What is it indicated for?
The Optima Coil System is intended for the endovascular embolization of intracranial aneurysms and other neurovascular abnormalities such as arteriovenous malformations and arteriovenous fistulae. The Optima Coil System is also intended for vascular occlusion of blood vessels within the neurovascular system to permanently obstruct blood flow to an aneurysm or other vascular malformation and for arterial and venous embolizations in the peripheral vasculature.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K200030 · printed Nov 6, 2026
Cite this page
510(k) Report. “K200030: Optima Coil System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K200030
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Record history
- FDA decision record loaded May 2, 2026
- Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026