Aesculap AG

6078 adverse events · 149 recalls · 64 clearances · 36 inspections · 2 compliance actions · aggregated across 6 source records

Scorecard

Events per device across the 25,238-device portfolio, trailing 12 months. Arrows compare the last 90 days with the 90 before.

MAUDE reports per device

0.017 ▼

429 in the last 12 months

Higher volume than 88% of companies with 10+ devices

Recalls per device

0.000 →

10 in the last 12 months

Higher volume than 98% of companies with 10+ devices

These are reporting-volume percentiles, not safety rankings — MAUDE counts have no denominator of devices in use, and recall attribution follows resolved links. A high percentile means more reports per registered device than peers, which can reflect market size, device criticality, or reporting practice as much as anything else.

Devices

25,238 device records · ordered by linked event volume.

Brand	Model	Product codes	Primary DI	Linked events
AESCULAP	PL574T	FZP	04046963398828	163
AS VEGA System® PS	NX053Z	JWH	04046963810412	158
AESCULAP	US751	FRG KCT	04038653473731	148
AESCULAP	PL579T	FZP	04046963398835	136
ENNOVATE	SZ378R	LXH	04046964719561	127
AESCULAP	PL572T	FZP	04038653208494	124
AESCULAP	GK384R	GEI	04038653172504	124
AS VEGA System® PS	NX055Z	JWH	04046963810450	124
AS VEGA System® PS	NX051Z	JWH	04046963810375	109
AESCULAP	NN260P	JWH	04046963711320	106
AS VEGA System® PS	NX031Z	JWH	04046963810160	104
PROGAV 2.0	FX643T	JXG	04041906502010	98
AESCULAP	PM438R	GEI HGI	04038653322862	97
S4 SPINAL SYSTEM	SW790T	MNI	04038653455256	87
ENNOVATE	SY001TS	NKB	04046964989728	85
M.BLUE PLUS	FX804T	JXG	04041906504793	85
AESCULAP	PL569T	FZP	04038653181353	82
AESCULAP	MD344	FRG KCT	14522281506819	79
AESCULAP	US906	JOJ	05055049007423	79
AS VEGA System® PS	NX009Z	JWH	04046963809867	79
AS	NX060Z	JWH	04046963655808	76
AS VEGA System® PS	NX011Z	JWH	04046963809904	74
AESCULAP	NX043	JWH	04046963810290	73
activL®	SW965	MJO	04038653430949	71
AS	NR400Z	KRO	04046963367732	67
AS VEGA System® PS	NX029Z	JWH	04046963810122	67
CRANIOPLATE	FM921T	JEY	04038653476527	65
M.BLUE	FX800T	JXG	04041906504397	61
PAS-PORT	FC700SU	FZP	04046955241026	60
AS VEGA System® PS	NX054Z	JWH	04046963810436	59

Showing 1–30 of 25,238Next →

Compliance actions

FDA warning letters and enforcement actions (full history).

Date	Type	Action	Firm
2011-09-26	WL	Warning Letter	Aesculap AG
2011-09-26	WL	Warning Letter	Aesculap AG

Facilities

Registered establishments with their latest FDA inspection outcome.

FEI	Name	Location	Last inspection
3002806315	AESCULAP AG	TUTTLINGEN, DONAU Baden-Wurttemberg, DE	NAI
3001354499	AESCULAP SAS	CHAUMONT Grand Est, FR	—
2916714	AESCULAP, INC.	CENTER VALLEY, PA, US	NAI
3003587896	AESCULAP, INC.	HAZELWOOD, MO, US	VAI
3008711893	B.Braun Medical (Suzhou) Co,.Ltd	Suzhou Jiangsu, CN	—