The Anspach Effort, Inc.
The Anspach Effort, Inc. holds FDA 510(k) medical device clearances, first cleared 1980, most recent 2022, with 261 FDA device recalls on record.
Top product codes for The Anspach Effort, Inc.
FDA recalls by The Anspach Effort, Inc.
10 most recent of 261- Z-0922-2023 — 7.5 cm Large Rotating Craniotome Attachment. Use with XMax¿, microMax, and eMax¿ Systems Ref: CRANI-L-R Intended for cutting and shaping bone including the spine and cranium
- Z-0923-2023 — 6.5 cm Pediatric Craniotome Attachment. Use with XMax¿, microMax, and eMax¿ Systems Ref: CRANI-P Intended for cutting and shaping bone including the spine and cranium
- Z-0920-2023 — 7.5 cm Large Craniotome Attachment Use with XMax¿, microMax, and eMax¿ Systems. Ref: CRANI-L Intended for cutting and shaping bone including the spine and cranium
- Z-0918-2023 — Adult Craniotome Ref: CRANI-A-G1 Intended for cutting and shaping bone including the spine and cranium
- Z-0917-2023 — 6.5 cm Adult Craniotome, Thin Foot Plate Attachment. Use with XMax¿, microMax, and eMax¿ Systems Ref: CRANI-A-01 intended for cutting and shaping bone including the spine and cranium by trained medical/surgical personnel
- Z-0921-2023 — Adult Craniotome, Large Ref: CRANI-L-G1 Intended for cutting and shaping bone including the spine and cranium
- Z-0919-2023 — 6.5 cm Adult Rotating Craniotome Attachment. Use with XMax¿, microMax, and eMax¿ Systems Ref: CRANI-A-R intended for cutting and shaping bone including the spine and cranium
- Z-0924-2023 — Pediatric Craniotome Ref:CRANI-P-G1
- Z-0916-2023 — 6.5 cm Adult Rotating Craniotome Attachment. Use with XMax¿, microMax, and eMax¿ Systems. Ref: CRANI-A Intended for cutting and shaping bone including the spine and cranium
- Z-0398-2018 — OSCILLATING SAW ATTACHMENT Surgical instrument motors and accessories/attachments are intended for use during surgical procedures to cut hard tissue or bone and soft tissue.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by The Anspach Effort, Inc.
- K220485 — Wireless Hand Control, EG1A (WIRELESS-HC), Receiver for Wireless Hand Control, EG1A (RECEIVER-HC)
- K183545 — Anspach Helix Dissection Tools
- K180063 — OCM-G1 Attachment
- K133604 — ANSPACH EG1 HIGH SPEED SYSTEM, G1 ATTACHMENTS
- K131053 — ANSPACH XMAX, EMAX2 AND EMAX2 PLUS SYSTEM WITH OTOLOGIC ATTACHMENT SYSTEM
- K113476 — ANSPACH DISSECTION TOOLS
- K082637 — CRANIAL PERFORATOR
- K080802 — EMAX 2 PLUS SYSTEM, MODEL EMAX 2 PLUS MOTOR, EMAX 2 CONSOLE>FIRMWARE UPGRADE, EMAX 2 FP FOOT PEDAL
- K061297 — ANSPACH IMRI SAFE SURGICAL DRILL SYSTEM
- K063688 — SURGICAL IRRIGATION SYSTEM, IRRIGATION TUBE
- K052572 — ANSPACH KNOTLESS ANCHOR
- K050628 — ANSPACH COUPLER
- K042783 — ANSPACH MINIMAL ACCESS SPINAL ATTACHMENT (MASA) SYSTEM
- K040186 — ANSPACH MRI SAFE SURGICAL DRILL SYSTEM
- K040076 — ANSPACH ADVANCED MICRO SAW ATTACHMENTS
- K030576 — ANSPACH IRRIGATION PUMP AND IRRIGATION PUMP II
- K022907 — ANSPACH POWERED KERRISON SYSTEM (PKS)
- K011444 — ANSPACH EMAX DRILL SYSTEM
- K002903 — ANSPACH ANGLED MICRONOSE ATTACHMENT
- K982991 — ANSPACH ACCESS CRANIAL PERFORATOR
- K981688 — ANSPACH SUTURE ANCHOR
- K974025 — ANSPACH SHIELDED ATTACHMENT
- K970530 — ANSPACH LUBRICATING SYSTEM II
- K965069 — ANSPACH SUTURE ANCHOR
- K965080 — ANSPACH MICROMAX SYSTEM
- K963686 — ANSPACH SUTURE ANCHOR (MODIFIED)
- K960630 — ANSPAHC SPEED REDUCER
- K955084 — ASPACH 65,000 (MODIFICATION)
- K945525 — ANSPACH SUTURE ANCHOR
- K940535 — AUTO LUBE SYSTEM
- K921338 — ANSPACH MINI-PLATING SYSTEM
- K864314 — EFTEKHAR RECHANNELIZATION DRILL GUIDE
- K852592 — CO2 FOR ARTHROSCOPY
- K850389 — MULTIPLE OUTLET MANIFOLD
- K841296 — TUBE TENDER
- K831756 — ANSPACH 65,000
- K830721 — WIRE TWISTERS
- K822065 — KAM SUCKER
- K820777 — MINI-MICRO ARTHROSCOPIC SCAPEL
- K820289 — ANTHROSCOPIC SURGICAL TABLE
- K820776 — CANNUOATED TROCHAR
- K820290 — SELF RETAINING RETRACTOR FOR HAND SURG
- K820291 — KNEE SUPPORT FOR X-RAY & SURGERY
- K820292 — EXTRACTOR III
- K820293 — BONE BIOPSY SET
- K820275 — ARTHROSCOPIC HARPOON
- K811996 — GATOR DRAPES
- K811717 — GATOR DRAPES
- K811115 — SUPERFLOW CANNULA FOR ARTHROS. SURGERY
- K811081 — MEDULLARY CANAL SCRAPERS
- K810303 — TELEVISION CAMERA HOLDER FOR SURGERY
- K803178 — ANSPACH MENISECTOMY KNIFE
- K802598 — CARBIDE CUTTING INSTRUMENT/INTRAARTICU
- K802599 — ARTHROSCOPIC FAT PAD RETRACTOR
- K802271 — THE IMMOBILIZER FOR OPEN & ARTHROSCOPIC
- K801326 — ANSPACH OPERATING TABLE SUPPORT/SPINAL
- K801330 — ANSPACH LEG SUPPORT
- K801327 — THE EXTRACTOR I TM
- K801328 — THE EQUALIZER
- K801329 — ANSPACH INSTRUMENT CADDY
Data sourced from openFDA. This site is unofficial and independent of the FDA.