Fresenius Medical Care: FDA 510(k) clearances across all its applicant names

FDA lists 201 510(k) clearances, 0 PMA and 0 De Novo decisions across the 11 applicant names Caduvo groups under Fresenius Medical Care, first 1984, latest 2026. Median 510(k) review time across these names: 116 days. Since 2017 the median was 168 days, against 180 days for all cleared 510(k)s in the same product codes. Groups are curated by Caduvo from public sources listed below; FDA does not group applicants. Counts include filings made before an acquisition, and can include older filings by a business that was later sold when FDA records them under the same applicant name; see the notes on this page.

510(k) clearances per year

YearClearancesMedian review days
20126124
201310163
201411104
20156111
2016288
20176124
2018790
20193178
20208267
20210—
20226257
20235230
20247184
202512116
20264152

The 11 FDA applicant names in this group

Applicant name510(k) clearancesPMADe NovoYears
Fresenius Medical Care Renal Therapies Group, LLC52002013–2026
Nxstage Medical, Inc.51002001–2024
Fresenius Medical Care North America42001998–2025
Fresenius USA, Inc.38001984–1999
Fresenius Medical Care7002000–2024
Fresenius Medical Care North America, Design Cente5002010–2013
Fresenius Medical Care South Asia Pacific Pty , Ltd.2002009–2011
Fresenius Medical Care, North America - Renal Ther1002014–2014
Fresenius Medical Care Reanal Therapies Group, LLC1002020–2020
Fresenius Medical Care Rental Therapies Group, LLC1002022–2022
Fresenius Medical Care-North America1002012–2012

Review time against the same product codes

Since 2017, 510(k)s cleared under these names took a median 168 days from FDA receipt to decision. All cleared 510(k)s in the same product codes over the same years took a median 180 days.

Top product codes

Product codeDeviceSubmissions510(k) clearances
KDIDialyzer, High Permeability With Or Without Sealed Dialysate System7575
KPODialysate Concentrate For Hemodialysis (Liquid Or Powder)2424
KDJSet, Administration, For Peritoneal Dialysis, Disposable1010
KOCAccessories, Blood Circuit, Hemodialysis1010
FKPSystem, Dialysate Delivery, Single Patient99
FKXSystem, Peritoneal, Automatic Delivery99
FIPSubsystem, Water Purification88
FJKSet, Tubing, Blood, With And Without Anti-Regurgitation Valve88
FKRSubsystem, Proportioning55
LKNSeparator, Automated, Blood Cell And Plasma, Therapeutic44

Plus 26 more product codes.

Review panels

Most recent Fresenius Medical Care 510(k) clearances

510(k)DeviceApplicant nameProduct codeDecision dateReview days
K261267Careflux H60;Careflux H70;Careflux V500Fresenius Medical Care Renal Therapies Group, LLCKDI2026-07-2499
K252377NxStage System One with NxViewFresenius Medical Care Renal Therapies Group, LLCKDI2026-05-15289
K252459multiFlux 130 (F00013123); multiFlux 160 (F00013124)Fresenius Medical Care Renal Therapies Group, LLCKDI2026-02-10189
K253462NaturaLyte® Dry Bicarbonate Concentrate (08-4112-2)Fresenius Medical Care Renal Therapies Group, LLCKPO2026-01-29114
K253518FX CorAL 40; FX CorAL 50Fresenius Medical Care Renal Therapies Group, LLCKDI2025-12-1836
K250634BCM2-Body Composition MonitorFresenius Medical Care Renal Therapies Group, LLCDSB2025-11-24266
K250471AquaC UNO HFresenius Medical Care Renal Therapies Group, LLCFIP2025-11-14269
K251851DIASAFEplusUS (F00013010)Fresenius Medical Care Renal Therapies Group, LLCFIP2025-10-09115
K252181AquaAFresenius Medical Care North AmericaFIP2025-09-0960
K252180Bicarby Dialysate RFP-404 (RFP-404-W); Bicarby Dialysate RFP-403 (RFP-403-W); Bicarby Dialysate RFP-403 (RFP-403-G); Bicarby Dialysate RFP-453 (RFP-453-W); Bicarby Dialysate RFP-453 (RFP-453-G); Bicarby Dialysate RFP-454 (RFP-454-W); Bicarby Dialysate RFP-454 (RFP-454-G); Bicarby Dialysate RFP-456 (RFP-456-W)Fresenius Medical Care Renal Therapies Group, LLCKPO2025-09-0960

191 earlier clearances. See the full list in Caduvo.

Recalls

82 product recalls in 44 recall events under these names; 11 initiated in the last five years.

Recalling firms are matched to the applicant names above by name only, so recalls filed under other names are not counted. A recall count says nothing about how safe one company's devices are compared with another's.

How this group is built

Groups are curated by Caduvo from public sources listed below; FDA does not group applicants. Counts include filings made before an acquisition, and can include older filings by a business that was later sold when FDA records them under the same applicant name; see the notes on this page.

Fresenius Medical Care and its US arm Fresenius USA, plus NxStage (2019). Includes filings made before the acquisition. Left out: Fresenius Kabi (a separate Fresenius SE business).

Sources

Frequently asked questions

How many FDA 510(k) clearances are listed across Fresenius Medical Care's applicant names?

FDA lists 201 510(k) clearances, 0 PMA and 0 De Novo decisions across the 11 applicant names Caduvo groups under Fresenius Medical Care, first 1984, latest 2026. FDA records each applicant name separately; Caduvo adds up the names listed on this page.

Which FDA applicant names does Fresenius Medical Care file under?

The names with the most 510(k) clearances in this group are Fresenius Medical Care Renal Therapies Group, LLC (52); Nxstage Medical, Inc. (51); Fresenius Medical Care North America (42); Fresenius USA, Inc. (38); Fresenius Medical Care (7). The full list of 11 names is on this page.

How long does FDA take to clear Fresenius Medical Care 510(k)s?

The median time from FDA receipt to decision across 510(k)s cleared under these names is 116 days. Since 2017 the median was 168 days, against 180 days for all cleared 510(k)s in the same product codes.

Does the Fresenius Medical Care count include acquired companies?

Yes. A group includes filings an acquired business made under its own name, including before the acquisition. Businesses that were sold are left out, and names whose ownership is unclear are not included. FDA does not group applicants; the sources for each grouping are listed on this page.

Next steps

Data from openFDA (510(k), PMA, De Novo, device recalls). Applicant names are matched exactly, with punctuation and legal suffixes removed. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this grouping or data.

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